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Health / Center for Devices and Radiological Health / Premarket approval / Medical device / Federal Food / Drug / and Cosmetic Act / Title 21 of the Code of Federal Regulations / Adverse event / Investigational Device Exemption / Unique Device Identification / Food and Drug Administration / Medicine / Technology


DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Document Control Room -WO66-G609
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Document Date: 2013-12-06 12:10:53

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File Size: 248,53 KB

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