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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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) Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 130,41 KB Share Document on Facebook

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