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Date: 2014-03-05 09:38:55 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 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 Avenue Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 41,98 KB Share Document on Facebook

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