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![]() Date: 2014-06-30 09:55:09Technology Center for Devices and Radiological Health Premarket approval Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Human cytomegalovirus Adverse event Investigational Device Exemption Medicine Food and Drug Administration Health | Source URL: www.accessdata.fda.govDownload Document from Source WebsiteFile Size: 44,14 KBShare Document on Facebook |