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U.S. Department of Health and Human Services

510(k) Premarket Notification
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61 to 70 of 490 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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Export all 490 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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nipro safetouch psv scalp vein set with safety device NIPRO MEDICAL CORPORATION K140136 02/14/2014
surflash safety i.v. catheter KOFU FACTORY OF TERUMO CORP. K141138 05/30/2014
i.v. catheter Jiangxi Sanxin Medtec Co., Ltd K142797 06/18/2015
supercath5 TOGO MEDIKIT CO., LTD. K140419 05/12/2014
accucath bc intravascular catheter system VASCULAR PATHWAYS, INC. K140504 07/17/2014
nexus midline ct catheter HEALTH LINE INTERNATIONAL CORPORATION K140270 08/20/2014
powerglide midline catheter C.R. BARD, INC. K133856 01/16/2014
terumo surflo i.v. catheter TERUMO (PHILIPPINES) CORPORATION K133280 06/12/2014
medsource iv safety catheter MEDSOURCE INTERNATIONAL, LLC. K131555 01/31/2014
argyle peripherally inserted central catheter single lumen, argyle peripherally inserted central catheter dual lumen COVIDIEN K132567 11/05/2013
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