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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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no. 5300-3 1/2 french umbilical vessel cath. etc. SUPERIOR PLASTIC PRODUCTS CORP. K851981 06/18/1985
sodium chloride solution SUPERIOR HEALTHCARE GROUP, INC. K903347 12/13/1990
biosensors central venous catheter kits SUNSCOPE INTL., INC. K002786 11/17/2000
sunder central venous catheter kit, models sd-3l55f30j and sd-3l70f30j SUNDER BIOMEDICAL TECH. CO., LTD. K024007 07/14/2003
specath central venous catheter kits SPECIAL MEDICAL CO. LTD. K021130 01/07/2003
viavalve safety iv catheter SMITHS MEDICAL ASD, INC. K113700 03/14/2012
viavalve safety i.v. catheter SMITHS MEDICAL ASD, INC. K160235 06/30/2016
advantiv safety i.v. catheter SMITHS MEDICAL ASD, INC. K072419 11/09/2007
wallace iv cannula SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. K932946 09/01/1995
wallace y-can SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. K932947 09/01/1995
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