medical device makers

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FDA Covers for Device Makers, Keeps Injuries Under Wraps

FDA Office of the Commissioner, Silver Spring, MD Medical Device News Desk, October 20, 2016 ~ The system is supposed to be transparent.   Medical device makers are required to alert the U.S. Food and Drug Administration (FDA) when their products injure consumers or malfunction.  The FDA then theoretically alerts [...]

By |2016-10-20T13:33:06+00:00October 20th, 2016|FDA News|4 Comments