Title 5 of the Code of Federal Regulations - PDFSEARCH.IO - Document Search Engine

Title 5 of the Code of Federal Regulations
Results: 241

#	Item
191	Kl~2t/ Attachment 5 OC 510(k) Summary 1. Submitter Information Name: Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-11-09 20:53:13 Health Medical equipment Food law Pharmaceuticals policy Center for Devices and Radiological Health Medical device Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Technology
192	X October 2011 David Conroy EPA - New England, Region I 5 Post Office Square, Suite 100 Boston, MA[removed]Dear Mr. Conroy: Add to Reading List Source URL: www.dem.ri.gov Language: English - Date: 2011-09-21 08:14:43 Clean Air Act United States Environmental Protection Agency New Source Review Air quality law National Ambient Air Quality Standards Air pollution Regulation of greenhouse gases under the Clean Air Act Title 40 of the Code of Federal Regulations Air pollution in the United States Environment Earth
193	DEC[removed]DvcInomto:Section 5: 510(k) Summary Comments Ouroboros Medical, Inc[removed]Fremont Blvd., Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-01-09 11:27:29 Endoscopy Neurosurgery Orthopedic surgery Premarket approval Medical device Federal Food Drug and Cosmetic Act Arthroscopy Discectomy Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Food law
194	510(k) SUMMARY 5 10(k) Owner: JN 521 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-02-17 14:36:25 Medical technology Food law Surgery Tissue expansion Medical device Federal Food Drug and Cosmetic Act Premarket approval Biocompatibility Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Medical equipment
195	1508 Federal Register / Vol. 66, No. 5 / Monday, January 8, [removed]Proposed Rules SUMMARY: The Food and Drug Administration (FDA) is proposing new Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 11:01:11 Pharmaceutical industry Pharmaceuticals policy Food safety Validity Allotransplantation Title 21 of the Code of Federal Regulations Center for Biologics Evaluation and Research Regulatory requirement Good manufacturing practice Medicine Health Food and Drug Administration
196	SECTION 5: 510(k) SUMMARY - JU Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-07-06 14:45:38 Technology Food law Pharmaceuticals policy Acne vulgaris 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
197	1/5 K1133!4 DCS Surgical, Inc. Page 1 of 3, Tab 5 Summary Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-12-06 10:15:16 Implants Medical equipment Interventional radiology Premarket approval Medical device Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Stent Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Food law
198	510(k) SUMMARY submitted in This summary of 5 10(k) safety and effectiveness information is being accordance with the requirements of SMDA 1990 and 21 CFR §[removed]OCT Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-11-28 00:37:42 Masks Food and Drug Administration Food law Code of Federal Regulations Polypropylene Premarket approval Medical device Title 21 of the Code of Federal Regulations Surgical mask Medicine Technology Medical equipment
199	EVERYWAY EVERYWAY MEDICAL INSTRUMENTS CO.,LTD. 311., No. 5, Lane 155, Sec. 3,Pcishen Rd, Shen Keng Hsiang, Taipei Hsien, Taiwan, FEB Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-03-26 00:30:44 Health Food law Medical equipment Clinical research Pharmaceutical industry Premarket approval Medical device Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Medicine Food and Drug Administration Technology
200	Interlace Medical Inc. k 1037q( 5. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-04-25 00:31:46 Food law Medical equipment Pharmaceuticals policy Medical device Medical technology Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Medicine Food and Drug Administration Health

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