Stewart & Stevenson’s Apollo ABVM Receives Emergency Use Authorization from U.S. Food and Drug Administration
Kirby Corporation (NYSE: KEX) announced that its subsidiary, Stewart & Stevenson Healthcare Technologies, received emergency use authorization from the FDA for the Apollo ABVM device during the COVID-19 pandemic. This device is designed for patients requiring mechanical ventilation in emergency situations when traditional ventilators are unavailable. The device can operate a common bag valve mask and is set for high-volume production, with manufacturing facilities located in Oklahoma City and Houston. This authorization marks a significant milestone for the Apollo ABVM program.
- FDA emergency use authorization for Apollo ABVM allows for manufacturing and distribution.
- Apollo ABVM provides a low-cost ventilation option for emergency situations.
- Manufacturing support from plants in Oklahoma City and Houston enhances operational flexibility.
- None.
HOUSTON, July 15, 2020 (GLOBE NEWSWIRE) -- Stewart & Stevenson Healthcare Technologies, LLC (“S&S”), a subsidiary of Kirby Corporation (“Kirby”) (NYSE: KEX), has received emergency use authorization for the Apollo ABVM from the U.S. Food and Drug Administration (“FDA”) for the duration of emergency circumstances caused by the COVID-19 pandemic1. With this authorization, the Apollo ABVM can now be used by patients during the COVID-19 pandemic for continuous or intermittent mechanical ventilation under the emergency use authorization guidelines.
The Apollo ABVM, which is based on a design created in Rice University’s Osman Engineering Design Kitchen, was refined by S&S to meet the standard for FDA emergency use authorization and make it ready for high volume production. It is an emergency device intended for healthcare professionals’ use to help patients breathe during first response situations when traditional, more complex ventilators are not available. The programmable device is designed to operate a common bag valve mask for extended periods of time under the supervision of a healthcare professional while patients await the availability of a traditional ventilator.
Joe Reniers, President of Kirby Distribution and Services commented, “The FDA authorization represents an important milestone achievement for the Apollo ABVM program. We can now commence manufacturing and distribution of this low-cost device to the frontlines, providing healthcare professionals with a sturdy and portable ventilation device for patients during the COVID-19 pandemic.” Several manufacturing sites supported these efforts, including manufacturing plants in Oklahoma City, OK and Houston, TX. “It is a testimony to the flexibility of our people and our manufacturing facilities that we are able to readily utilize operations to support COVID-19 related needs,” added Reniers.
Stewart & Stevenson, LLC a subsidiary of Houston-based Kirby Corporation and founded in 1902, is focused on manufacturing, power generation, rental solutions and aftermarket support for global oil and gas, marine, construction, transportation, government, mining, health care and agricultural markets. S&S, composed of Manufacturing Technologies, Power Products, Atlantic Detroit Diesel-Allison, Florida Detroit Diesel-Allison, S&S Colombia, Healthcare Technologies and Power Rental, serves customers worldwide from 43 U.S. and international locations.
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1 This product has not been FDA cleared or approved, it has been authorized by FDA under EUA
Contact: Chad Joost 281-345-5151
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