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Center for Devices and Radiological Health
Results: 3105

#	Item
331	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service __________________________________________________________________________________________________________________________ Food and Drug Administration[removed]N Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-06 09:56:08 Health Medical device Center for Devices and Radiological Health Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Quality management system Code of Federal Regulations Title 21 CFR Part 11 Medicine Food and Drug Administration Technology
332	Advisory Committee Meeting, September 23, 2014 Bethesda Marriott Hotel 5151 Pooks Hill Rd., Bethesda, MD 20814, [removed]AGENDA 8:00 am Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical pharmacology Therapeutics United States Public Health Service Center for Devices and Radiological Health Adverse event Biometrics Bethesda Maryland Levofloxacin Pharmaceutical sciences Pharmacology Clinical research
333	RERC on Accessible Medical Instrumentation Add to Reading List Source URL: www.fda.gov Language: English Health Premarket approval Investigational Device Exemption Medical device Center for Devices and Radiological Health Humanitarian Device Exemption Usability Human factors Food and Drug Administration Medicine Technology
334	Humanitarian Device Exemptions Nicole Wolanski CAPT, USPHS Director, Premarket Approval Section Add to Reading List Source URL: www.fda.gov Language: English Health Humanitarian Device Exemption Premarket approval Clinical trial Center for Devices and Radiological Health Food and Drug Administration Pharmaceutical sciences Medicine
335	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:41:56 Health Medical device Premarket approval Center for Devices and Radiological Health 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
336	FDA Patient Safety News: Show #55, September 2006 Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmaceutical industry Adverse event Clinical research Duragesic Fentanyl Center for Devices and Radiological Health Transdermal patch Adverse Event Reporting System Medicine Food and Drug Administration Pharmacology
337	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service __________________________________________________________________________________________________________________________ SOPRO-Acteon Group Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-06 09:56:04 Technology Food law Pharmaceuticals policy Medical equipment Medical device Medical technology Center for Devices and Radiological Health Premarket approval Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Health
338	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-06 09:57:07 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Quality management system Code of Federal Regulations Title 21 CFR Part 11 Medicine Food and Drug Administration Technology
339	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. It was current when produced, but is no longer maintained and may Add to Reading List Source URL: www.fda.gov Language: English Technology Joshua Sharfstein Center for Devices and Radiological Health Medical device Question Big: the musical Food and Drug Administration Medicine Health
340	Classification Discussion of Iontophoresis Devices Not Labeled for Use with a Specific Drug 21 CFR[removed]b) Add to Reading List Source URL: www.fda.gov Language: English Electrophoresis Iontophoresis Health Medical device Hyperhidrosis Center for Devices and Radiological Health Premarket approval Medicine Food and Drug Administration Technology

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