HeartBeam Reports Third Quarter 2022 Financial Results
HeartBeam, Inc. (NASDAQ: BEAT) announced the submission of its HeartBeam AIMI™ platform for FDA clearance, enhancing its heart attack detection technology. The company also plans to submit the AIMIGo telehealth solution by Q4 2022. With two new patents granted, HeartBeam aims to expand its product pipeline to include smartwatch connectivity. Financially, the company reported a net loss of $3.6 million for Q3 2022, up from $1.2 million the previous year, with research and development expenses reaching $1.6 million. Cash reserves stood at $6.5 million as of September 30, 2022.
- FDA submission for HeartBeam AIMI platform enhances market position.
- Two new patents add protection and potential for product expansion.
- Strong conviction in AIMI and AIMIGo technology suggests future growth.
- Net loss increased to $3.6 million in Q3 2022, indicating financial pressure.
- R&D expenses rose significantly to $1.6 million, impacting profitability.
- Cash position decreased to $6.5 million, raising concerns about funding.
HeartBeam AIMI™ Platform Technology for use in Diagnosing Heart Attacks Submitted to FDA for Clearance
Company on Track for Initial FDA Submission of HeartBeam AIMIGo™, the Telehealth Solution, in Q4 2022
AIMIGo Technology Receives Two Additional Patents
Company Plans to Broaden Product Portfolio Pipeline with Smartwatch Connectivity
Management to Host Webcast and Conference Call Today At
Third Quarter and Subsequent 2022 Operational Highlights
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Announced the
US Food and Drug Administration (FDA) 510(k) application submission of HeartBeam AIMI platform, seeking approval for the Company’s proprietary VECG technology to aid in diagnosis of heart attack in total addressable market$500 million - Broadened product portfolio pipeline with smartwatch connectivity supporting a daily multi-hour heart monitoring solution, leveraging the HeartBeam AIMIGo platform to address the multibillion-dollar global market for detection of atrial arrhythmias
- Granted patent for signal transformation from VECG to 12-Lead Electrocardiogram (ECG), allowing the HeartBeam AIMIGo credit card-sized device to enable a 12-lead ECG anytime, anywhere
- Granted patent for 12-lead ECG patch monitor intended for detection of heart attacks and complex cardiac arrhythmias, opening a pathway to a disruptive ischemia and arrhythmia detection via 12-lead ECG patch product
- Expanded the addressable patient population for the Company’s HeartBeam AIMI software platform to provide access to a broader patient population in the emergency care setting
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Appointed
Peter J. Fitzgerald , MD, PhD, as Chief Medical Officer, a renownedStanford cardiologist who brings deep clinical, research, and industry expertise to the executive team -
Appointed healthcare and cardiac industry veteran,
Ken Persen , to the role of Chief Technology Officer -
Selected as winner of the annual Cardiovascular Innovations (CVI) 2022
Innovation Summit and Shark Tank Competition , an annual awards program recognizing innovative state-of-the-art cardiac technologies -
Presented at investor conferences including the LD Micro Main Event
XV, Dawson James Small Cap Growth Conference andThinkEquity Conference , and hosted a virtual roadshow webinar during whichHeartBeam unveiled a new video featuring the HeartBeam AIMI and AIMIGo Technology - Unveiled new video featuring the HeartBeam AIMI and AIMIGo Technology, available here
Management Commentary
“Throughout the third quarter we progressed on our commercialization pathway toward a series of important milestones, including the FDA 510(k) application submission of our HeartBeam AIMI product,” said
“The issuance of two patents during the quarter provided further intellectual property protection for the
“A second patent that enables generation of a synthesized 12-lead ECG by the HeartBeam AIMIGo credit card-sized device opens a pathway for a patient to record a set of signals using HeartBeam AIMIGo outside of a medical setting with a diagnostic synthesized 12-lead ECG immediately transmitted to a clinician for review and diagnosis. Unlike single-lead ECG products currently in the marketplace such as other credit card sized devices or smartwatches, the
“Operationally, during the quarter we welcomed
“Looking ahead, our commercialization path is on track with our AIMIGo 3D vector ECG first-generation product expected to be ready for FDA submission in the fourth quarter of this year, along with FDA clearance for HeartBeam AIMI. Our commercial team has continued to engage in positive discussions with strategic institutions, including academic centers, regional healthcare systems, and regional community hospital systems. We look forward to providing updates on our progress in the months ahead,” concluded
Key Milestones
-
HeartBeam AIMI Platform
- Development of FDA-Ready Product Completed – Q2 2022
- FDA Study Completed – Q3 2022
- FDA Submission Completed – Q3 2022
- FDA Clearance – Q4 2022
- Limited Market Release – Q1 2023
- Product Launch – Q2 2023
-
HeartBeam AIMIGo Device
- Development of FDA-Ready V1 Product Completed – Q3 2022
- FDA Submission V1 – Q4 2022
- FDA Clearance V1 – Q1 2023
- Limited Market Release V1 – Q2 2023
- Development of FDA-Ready V2 Product Completed– Q2 2023
- FDA Study V2 – Q2 2023
- FDA Submission V2 – Q2 2023
- FDA Clearance V2 – Q3 2023
- Limited Market Release V2 – Q4 2023
- Product Launch – Q1 2024
Third Quarter 2022 Financial Results
Research and development expenses for the third quarter of 2022 were
General and administrative expenses for the third quarter of 2022 were
Net loss for the third quarter of 2022 was
Cash totaled
Third Quarter 2022 Results Conference Call
To access the call, please use the following information:
Date: |
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Time: |
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Dial-in: |
1-800-458-4121 |
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International Dial-in: |
1-646-828-8193 |
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Conference Code: |
7787050 |
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Webcast: |
https://viavid.webcasts.com/starthere.jsp?ei=1576186&tp_key=0aec66c6b6 |
A telephone replay will be available approximately two hours after the call and will run through
About
Forward-Looking Statements
All statements in this release that are not based on historical fact are "forward-looking statements." While management has based any forward-looking statements included in this release on its current expectations, the information on which such expectations were based may change. Forward-looking statements involve inherent risks and uncertainties which could cause actual results to differ materially from those in the forward-looking statements, as a result of various factors including those risks and uncertainties described in the Risk Factors and in Management’s Discussion and Analysis of Financial Condition and Results of Operations sections of our in our Forms 10-K, 10-Q and other reports filed with the
Balance Sheets (Unaudited) (In thousands, except share data) |
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Assets |
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Current Assets: |
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Cash and cash equivalents |
$ |
6,549 |
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$ |
13,192 |
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Prepaid expenses and other assets |
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123 |
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806 |
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Total Assets |
$ |
6,672 |
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$ |
13,998 |
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Liabilities and Stockholders’ Equity |
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Current Liabilities: |
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Accounts payable and accrued expenses (includes related party |
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932 |
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588 |
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Total Liabilities |
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932 |
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588 |
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Commitments and contingencies (Note 7) |
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Stockholders’ Equity |
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Common stock - |
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1 |
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1 |
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Additional paid in capital |
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24,213 |
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22,633 |
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Accumulated deficit |
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(18,474 |
) |
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(9,224 |
) |
Total Stockholders’ Equity |
$ |
5,740 |
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$ |
13,410 |
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Total Liabilities and Stockholders’ Equity |
$ |
6,672 |
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$ |
13,998 |
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Statements of Operations (Unaudited) (In thousands, except share and per share data) |
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Three months ended
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Nine months ended
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2022 |
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2021 |
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2022 |
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2021 |
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Operating Expenses: |
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General and administrative |
$ |
2,048 |
|
|
$ |
341 |
|
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$ |
5,256 |
|
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$ |
785 |
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Research and development |
|
1,562 |
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|
|
105 |
|
|
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4,036 |
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|
|
159 |
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Total operating expenses |
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3,610 |
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446 |
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9,292 |
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944 |
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Loss from operations |
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(3,610 |
) |
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(446 |
) |
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(9,292 |
) |
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(944 |
) |
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Other Income (Expense) |
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Interest income (expense) |
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28 |
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|
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(742 |
) |
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39 |
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|
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(1,421 |
) |
Other income |
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3 |
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|
— |
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|
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3 |
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|
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22 |
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Total other income (expense) |
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31 |
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|
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(742 |
) |
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42 |
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|
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(1,399 |
) |
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Loss before provision for income taxes |
$ |
(3,579 |
) |
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$ |
(1,188 |
) |
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$ |
(9,250 |
) |
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$ |
(2,343 |
) |
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Income tax provision |
$ |
— |
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$ |
— |
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$ |
— |
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$ |
— |
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Net Loss |
$ |
(3,579 |
) |
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$ |
(1,188 |
) |
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$ |
(9,250 |
) |
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$ |
(2,343 |
) |
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Net loss per share, basic and diluted |
$ |
(0.44 |
) |
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$ |
(0.32 |
) |
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$ |
(1.14 |
) |
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$ |
(0.63 |
) |
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Weighted average common shares outstanding, basic and diluted |
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8,147,024 |
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3,720,880 |
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8,107,359 |
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3,706,001 |
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Statements of Cash Flows (Unaudited) (In thousands) |
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Nine Months ended |
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2022 |
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2021 |
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Cash Flows From Operating Activities |
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Net loss |
$ |
(9,250 |
) |
|
$ |
(2,343 |
) |
Adjustments to reconcile net loss to net cash used in operating activities |
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Accretion expense, convertible notes |
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— |
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|
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1,187 |
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Non-cash interest expense |
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— |
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233 |
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Stock-based compensation expense |
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774 |
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|
85 |
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PPP loan forgiveness |
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— |
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(22 |
) |
Changes in operating assets and liabilities: |
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Prepaid expenses and other current assets |
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683 |
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(139 |
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Accounts payable and accrued expenses |
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800 |
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|
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210 |
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Net cash used in operating activities |
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(6,993 |
) |
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(789 |
) |
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Cash Flows From Financing Activities |
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Proceeds from sale of equity |
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348 |
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|
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— |
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Proceeds from exercise of stock options |
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2 |
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— |
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Proceeds from issuance of convertible notes |
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— |
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|
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1,560 |
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Net cash provided by financing activities |
|
350 |
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|
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1,560 |
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Net (decrease) increase in cash |
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(6,643 |
) |
|
|
771 |
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Cash and Cash Equivalents – Beginning of period |
|
13,192 |
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|
|
24 |
|
|
|
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Cash and Cash Equivalents – Ending of period |
$ |
6,549 |
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|
$ |
795 |
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Supplemental Disclosures of Cash Flow Information: |
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Taxes paid |
$ |
— |
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$ |
— |
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Supplemental Disclosures of Non-cash Financing Activities: |
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Issuance of common stock and warrants to settle accrued expenses |
$ |
456 |
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$ |
— |
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Conversion of short-term notes to convertible notes |
$ |
— |
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$ |
1,856 |
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View source version on businesswire.com: https://www.businesswire.com/news/home/20221110006054/en/
Investor Relations Contact:
Executive Vice President
Direct: 949-491-8235
BEAT@mzgroup.us
www.mzgroup.us
Media Contact:
media@capwellcomm.com
949-999-3303
Source:
FAQ
What recent developments has HeartBeam (BEAT) made regarding FDA submissions?
How did HeartBeam's (BEAT) financial results for Q3 2022 compare to Q3 2021?