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Date: 2014-03-05 09:38:55Health 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 Quality management system Investigational Device Exemption Food and Drug Administration Medicine Technology | DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire AvenueAdd to Reading ListSource URL: www.accessdata.fda.govDownload Document from Source WebsiteFile Size: 41,98 KBShare Document on Facebook |
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