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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 57 Results
ProductCode: DTQ Decision Date To: 09/29/2016
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Export all 57 Records to ExcelExport to Excel | Download Files | More About 510(k)
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stockert compact system STOECKERT INSTRUMENTE K982014 09/04/1998
interface module iddd STOECKERT INSTRUMENTE K992635 12/20/1999
a-miniature centrifugal blood pump system, model cpb 2000 A-MED SYSTEMS, INC. K992592 05/04/2000
s3 cardioplegia control module version 2.0 MEDICAL DEVICE CONSULTANTS, INC. K002116 08/09/2000
stockert compact system version 2.0 STOECKERT INSTRUMENTE K002118 08/09/2000
siii alarm amplifier STOCKERT INSTRUMENTE GMBH K011088 05/02/2001
cardiovention powerbase console, model pbc-100 CARDIOVENTION, INC. K021694 01/08/2003
advanced perfusion system 1 (100/120 volt),advanced perfusion system 1 (220/240 volt, roller pumps (6, 4 inch TERUMO CARDIOVASCULAR SYSTEMS CORP. K022947 03/20/2003
stockert centrifugal pump console STOCKERT INSTRUMENTE GMBH K020571 09/23/2002
modification to cardiovention powerbase console, model pcb-100 CARDIOVENTION, INC. K030141 02/26/2003
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