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Center for Devices and Radiological Health
Results: 3105

#	Item
641	JUN[removed] %WkJY1 Traditional 510(k) NEOTIS System Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-07-18 16:17:23 Health Food law Pharmaceutical industry Medical equipment Pharmaceuticals policy Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Technology
642	Federal Register / Vol. 79, No[removed]Friday, July 25, [removed]Rules and Regulations DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 876 [Docket No. FDA–2012–N–0303] Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-07-25 03:04:32 Health Food law Pharmaceuticals policy Medical equipment Medical device Premarket approval Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Medical technology
643	NWX-HHS FDA (US) Moderator: Irene Aihie[removed]:31 pm CT Confirmation # [removed]Page 1 Add to Reading List Source URL: www.fda.gov Language: English Technology Medical device Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Predicate Medicine Food and Drug Administration Health
644	DEPARTMENT OF HEALTH & HUMAN SERVICES June 24, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-07-23 14:57:59 Technology 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 Health
645	P130030_Approval_Order.pdf Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-07-23 08:36:17 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
646	[removed]Federal Register / Vol. 79, No[removed]Tuesday, August 5, [removed]Notices III. Electronic Access Persons interested in obtaining a copy Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-10-07 08:58:36 Pharmaceutical sciences Biosimilar Biologic License Application Center for Biologics Evaluation and Research Biologic Center for Devices and Radiological Health Center for Drug Evaluation and Research Food and Drug Administration Medicine Clinical research
647	DEPARTMENT OF HEALTH & HUMAN SERVICES DEC 7 Food and Drug Administration Center for Devices and Add to Reading List Source URL: www.fda.gov Language: English - Date: 2004-12-27 14:08:58 Food and Drug Administration Entertainment Laser lighting display Visual music Center for Devices and Radiological Health Laser Title 21 of the Code of Federal Regulations Variance Medicine Optics Statistics
648	Microsoft Word - Document1 Add to Reading List Source URL: www.aami.org Language: English - Date: 2014-07-31 15:14:12 Health Underwriters Laboratories Medical device Battery Food and Drug Administration Lithium battery Center for Devices and Radiological Health Medicine Technology Standards organizations
649	Ki140564 Page 1 of[removed]k) Summary JUN 0 5 20i14 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-07-18 16:17:48 Health Food law Pharmaceutical industry Pharmaceuticals policy Clinical research Medical device Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Premarket approval Medicine Food and Drug Administration Technology
650	JUL[removed]NUV r\SIVE-Traditional paeo,n[removed]K140479 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-08 12:37:18 Food law Pharmaceuticals policy Medical equipment Neurosurgery Medical device Federal Food Drug and Cosmetic Act Premarket approval Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Health

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