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U.S. Department of Health and Human Services

510(k) Premarket Notification
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71 to 80 of 489 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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510(K)
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mini-midline extended dwell safety catheter LUTHER NEEDLESAFE PRODUCTS, INC. K130518 04/30/2013
jms safe wing cath (swc) JMS NORTH AMERICA CORPORATION K121488 03/05/2013
bd nexiva diffusics closed iv catheter system BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. K123734 01/17/2013
neo delta self safe t, neo delta self safe t, neo delta self safe 1, neo delta self safe 1 DELTA MED SRL K121007 12/28/2012
surfflash(r) plus safety i.v. catheter KOFU FACTORY OF TERUMO CORP. K123267 11/02/2012
terumo surflash safety i.v. catheter TERUMO Corporation K122544 09/05/2012
novacath secure iv catheter system-18g TANGENT MEDICAL TECHNOLOGIES, INC. K120839 07/20/2012
m/29tm - pressure injectable FLEXICATH LTD. K111939 07/11/2012
powerglide midline catheter C.R. BARD, INC. K121073 06/01/2012
orion ii ct cvc HEALTH LINE INTERNATIONAL CORPORATION (HLIC) K113622 05/18/2012
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