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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 09/26/2016
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Export all 185 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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u & u intravascular administration set U & U Medical Technology Co., Ltd K151151 09/24/2015
tutoplus iv administration set MYCO MEDICAL SUPPLIES, INC. K990388 03/29/1999
tutodrop 1 and tutodrop 2 MYCO MEDICAL SUPPLIES, INC. K982098 03/01/1999
tk intravascular administration set Anhui Tiankang Medical Technology Co.,Ltd. K191640 08/26/2020
three way infusion set MED FUSION SYSTEMS, INC. K841882 06/05/1984
tamaryn i.v. flow regulator extension set TAMARYN MEDICAL SYSTEMS, INC. K971066 06/04/1997
sterile i.v. start kit ORION LIFE SYSTEMS, INC. K902810 11/13/1990
standard administration sets 3M COMPANY K885030 01/24/1989
specialty set model iv7a01 VALLEYLAB, INC. K830891 04/14/1983
spark kit(r), modification LYPHOMED, INC. K910142 05/14/1991
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