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Date: 2013-12-06 12:10:53 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 Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 248,53 KB Share Document on Facebook

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