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ISO 10993
Results: 77

#	Item
31	CYBERSONICS ABBREVIATED 510(k) SUBMISSION Cyber~and Dual Action Ultrasonic Lithotripsy System K120303IS001 5MD(14 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-07-06 14:44:12 Medical ultrasound Sensors Extracorporeal shock wave lithotripsy Ultrasonic sensor Lithotripsy ISO 10993 Medical device Sterilization Ethylene oxide Medicine Medical equipment Ultrasound
32	c 1a Reverse Medical CorporationY~90T\? Reverse Medical Microcatheter 510(k) Submission[removed]k) Summary according to[removed] Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-01-09 11:27:22 Surgery Catheters Medical device Medical technology Port Percutaneous Biocompatibility ISO 10993 Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Medical equipment
33	510(k) Summary Submitter: Arteriocyte Medical Systems, Inc. 45 South Street Hopkinton, MA 01748 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-11-14 08:33:44 Health Medical equipment Pharmaceuticals policy Food law Medical technology Medical device Premarket approval ISO 10993 Title 21 CFR Part 11 Medicine Food and Drug Administration Technology
34	Unimax Medical Systems Inc[removed]k) Notification1 uiG Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-10-31 00:33:01 Technology Anti-fog Medical device Fog Federal Food Drug and Cosmetic Act Laparoscopic surgery Premarket approval Quality management system ISO 10993 Medicine Health Food and Drug Administration
35	LA.J ASAPLP K[removed]k) Summary Aspiration Catheter Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-09 11:45:36 Food and Drug Administration Medical equipment Food law Catheters Medical device Premarket approval ISO 10993 Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Medicine Medical technology Technology
36	EC 2.7 Endoscopic Cutter Medtronic Advanced Energy LLC Traditional 510(k) NO Add to Reading List Source URL: www.accessdata.fda.gov Language: English* - Date: 2012-12-06 10:13:14 Food and Drug Administration Medical equipment Pharmaceutical industry Food law Pharmaceuticals policy Medical device Electrosurgery ISO 10993 Center for Devices and Radiological Health Medicine Health Technology
37	Oreatbatch Medical Traditional Premnarket Notification 510(k) MohiCath Transseptal Needle 00G reatbatch~ 1000Medical Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-11-28 00:37:58 Technology Cannula Port ISO 10993 Title 21 CFR Part 11 Medicine Medical equipment Medical technology
38	PDF Document Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-03-26 00:30:20 Food law Medical technology Medical equipment Medical device Pharmaceutical industry ISO 10993 Validation Laparoscopic surgery Premarket approval Medicine Health Food and Drug Administration
39	Traditional 510(k) for Rocket IPC System Q Rocketmedical The eCopy is an exact duplicate of the paper copy; Rev ised 510(k) K123033 SUMMARY Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-03-08 15:18:02 Catheters Pleural effusion Chest tube Malignant pleural effusion Port Pleural cavity Medical device Pleurodesis ISO 10993 Medicine Medical equipment Medical technology
40	Ic[removed]___________MAR Exhibit F[removed] Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-04-11 12:53:21 Food law Traumatology Medical equipment Medical technology Medical device Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Ultrasound ISO 10993 Medicine Health Food and Drug Administration

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