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Nathan Reeves on Food and Drug Administration (FDA) | JD Supra
JD Supra· 13 hours agoThis Privacy Policy describes how JD Supra, LLC ("JD Supra" or "we," "us," or "our") collects, uses and shares personal data collected from visitors to ...
FDA recalls Abbott’s HeartMate 3 ventricular assist device after 2 deaths
Medical Device Network via Yahoo Finance· 3 hours agoThe US Food and Drug Administration (FDA) has tagged a recall of Abbott’s HeartMate 3 left...
FDA report highlights need to improve diversity in clinical trials
Clinical Trials Arena via Yahoo Finance· 6 hours agoThe US Food and Drug Administration’s (FDA) Center for Drug Evaluation
San Diego's Cue Health had the first FDA-approved home COVID-19 test. Now the agency says to throw...
U-T San Diego· 1 day agoThe U.S. Food and Drug Administration told consumers Monday to throw out any at-home COVID-19 tests...
FDA approves Bristol Myers Squibb’s Breyanzi for follicular lymphoma
Pharmaceutical Technology via Yahoo Finance· 8 hours agoThe US Food and Drug Administration (FDA) has granted accelerated approval for Bristol Myers Squibb...
Getinge to limit US sales of heart devices after FDA safety warning
MedTech Dive via Yahoo Finance· 7 hours ago“It is related to working through the challenges on the balloon pump itself. There's some technical ...
Atraverse receives approval for HOTWIRE Left Heart Access Device
Medical Device Network via Yahoo Finance· 8 hours agoAtraverse Medical has received the US Food and Drug Administration (FDA) clearance for its HOTWIRE...
Axogen begins FDA submission for nerve graft product By Investing.com
Investing.com· 5 hours agoAxogen, Inc. (NASDAQ: AXGN), a company specializing in surgical solutions for peripheral nerve...
Study investigates cardiac cell regeneration in search of novel therapeutics
Medical Xpress· 37 minutes agoWith that in mind, Mahmoud Salama Ahmed, Ph.D., and an international team of researchers have completed an investigation to uncover novel therapeutics or existing therapeutic ...
Ventilator recall issued with warning of "serious injuries or death"
Newsweek· 1 day agoThe U.S. Food and Drug Administration (FDA) has ordered a software recall for a type of ventilator...