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Clinical research / Health / Pharmaceutical industry / Pharmacology / Therapeutics / Center for Devices and Radiological Health / Medical device / Adverse event / Clinical trial / Medicine / Food and Drug Administration / Pharmaceutical sciences


PLAN OF ACTION FOR IMPLEMENTATION OF 510(K) AND SCIENCE RECOMMENDATIONS   In August 2010, the Food and Drug Administration’s Center for Devices and Radiological Health (CDRH or the Center) 
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