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U.S. Department of Health and Human Services

510(k) Premarket Notification
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41 to 50 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 08/29/2016
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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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lectrospiral VYGON CORP. K883612 09/29/1988
vygon bionector with extension set VYGON CORP. K963981 02/14/1997
disposable plastic transfus./infus. assb VALLEYLAB, INC. K822354 09/22/1982
model iv 1500 standard burette VALLEYLAB, INC. K781637 12/12/1978
specialty set model iv7a01 VALLEYLAB, INC. K830891 04/14/1983
valleylab i.v. administration sets VALLEYLAB, INC. K883318 10/21/1988
mr extension set (001) UNIVERSITY OF MICHIGAN K964968 02/27/1997
iv administration set U.S. SAFETY SYRINGES CO., INC. K080660 05/13/2008
novolet U.S. SAFETY SYRINGES CO., INC. K080665 05/13/2008
u & u intravascular administration set U & U Medical Technology Co., Ltd K151151 09/24/2015
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