Date: 2010-12-01 11:49:36Premarket approval Medical device Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations National Institutes of Health Administration of federal assistance in the United States ClinicalTrials.gov Unique Device Identification Medicine Food and Drug Administration Health | | [removed]Federal Register / Vol. 69, No[removed]Friday, May 21, [removed]Notices (6), Title 5 U.S.C., and the Determination of the Director, Management Analysis andAdd to Reading ListSource URL: www.gpo.govDownload Document from Source Website File Size: 178,76 KBShare Document on Facebook
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