Statement from FDA Commissioner Scott Gottlieb, M.D. and Jeff Shuren, M.D., Director of the Center for Devices and Radiological Health, on latest steps to strengthen FDA’s 510(k) program for premarket review of medical devices - FDA Press Releases

FDA takes more steps toward strengthening 510(k) program for premarket review of medical devices

from Food and Drug Administration--Press Releases http://bit.ly/2MoaoPW
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