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Notification Center
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#	Item
461	Merit Medical Systems, Inc. Merit Marquis Flow Switch Traditional Premarket Notification 51 0(k) UL-I2011 Section 5. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-08-29 00:30:12 Health Food law Medical equipment Pharmaceuticals policy Pharmaceutical industry Medical device Premarket approval Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Medicine Food and Drug Administration Technology
462	This summary of 5 10(k) safety and effectiveness information is submitted in accordance with the requirements of the Safe Medical Devices Act of 1990 and 21 CFR §[removed]The submitter of this premarket notification is: Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-02-17 14:37:05 Food law Pharmaceuticals policy Medical technology Medical device Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Medical monitor Medicine Food and Drug Administration Medical equipment
463	ORIGINAL, TRADITIONAL 510(K) NOTifICATION PERMOBIL POWERED WHEELCHAIR: M3001M400MA-320 KOL? 510(k) Snnmnary Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-04-25 00:31:08 Health Food law Pharmaceuticals policy Medical equipment Medical device Medical technology Premarket approval Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Medicine Food and Drug Administration Technology
464	MAR L.D Technology LLC. 510(k) Premarket Notification Number: K[removed]Preparation date: September, 21 2Q11 510(k) Summary Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-04-23 00:33:51 Health Food law Medical technology Medical equipment Medical device Contec Medical Systems Validation Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medicine Technology Food and Drug Administration
465	Traditional 510(k) Premarket Notification Submission: Creganna-Tactx T . Steerable Sheath Set Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-09-13 12:40:25 Health Food law Pharmaceutical industry Pharmaceuticals policy Clinical research Medical device Federal Food Drug and Cosmetic Act Premarket approval Center for Devices and Radiological Health Medicine Food and Drug Administration Technology
466	ki/L) 72Ce Premarket Notification 5 10(k) Section[removed]k) Summary Tacker Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-07-25 00:34:04 Premarket approval Medical device Federal Food Drug and Cosmetic Act IMesh Hernia Center for Devices and Radiological Health Invasiveness of surgical procedures Surgery Medicine Health Food and Drug Administration
467	WI~ ~FEB-S3 510(K) PREMARKET NOTIFICATION SUMMARY This summary of 5lO(k) safety and effectiveness information is being submitted in accordance with Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-03-07 11:36:53 Food law Medical equipment Medical technology Implants Medical device Federal Food Drug and Cosmetic Act Premarket approval Abutment Center for Devices and Radiological Health Medicine Health Food and Drug Administration
468	Oculus Innovative Sciences 1129 N. McDowell Blvd. Petaluma, CA[removed]k) Premarket Notification K[removed]EpicynTM" HydroGel Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-03-07 11:37:03 Technology Food law Premarket approval Medical device Federal Food Drug and Cosmetic Act Gel Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Health
469	ArthroCar" Corporation Premarket Notification SMARTSTITC-I PERFECTPASSER® SYSTEM 1 General Information Submitter Name/Address Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-12-06 10:13:46 Health Food law Pharmaceuticals policy Medical equipment Code of Federal Regulations Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Technology
470	Covidlen 510(k) Premarket Notification 510(k) Summary of Safety and Effectiveness Qe 13 MY Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-06-11 00:36:20 Food law Pharmaceuticals policy Premarket approval Medical device Federal Food Drug and Cosmetic Act Laparoscopic surgery Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Clip Medicine Food and Drug Administration Health

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