Date: 2014-05-29 06:03:01Technology Premarket approval Medical device Prescription Drug User Fee Act Investigational Device Exemption Structured Product Labeling Unique Device Identification Food and Drug Administration Medicine Health | | [removed]Federal Register / Vol. 79, No[removed]Thursday, May 29, [removed]Notices to meet current standards, the Agency will advise ANDA applicants to submitAdd to Reading ListSource URL: www.gpo.govDownload Document from Source Website File Size: 202,53 KBShare Document on Facebook
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