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U.S. Department of Health and Human Services

510(k) Premarket Notification

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1 to 10 of 11 Results
ProductCode: DWF Applicant: HEARTPORT, INC. Decision Date To: 05/18/2022
 
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quickdraw venous cannula HEARTPORT, INC. K981995 04/20/1999
heartport endovenous drainage cannula HEARTPORT, INC. K962835 02/10/1997
heartport endosinus catheter HEARTPORT, INC. K961270 06/18/1996
heartport endopulmonary vent catheter HEARTPORT, INC. K981009 09/04/1998
heartport endopulmonary vent HEARTPORT, INC. K961245 06/18/1996
heartport endocoronary sinus cathetr HEARTPORT, INC. K964248 01/22/1997
heartport endoarterial return cannula HEARTPORT, INC. K971291 06/17/1997
heartport endoarterial return cannual HEARTPORT, INC. K955121 05/10/1996
heartport direct aortic return cannula with introducer HEARTPORT, INC. K974736 07/15/1998
directflow kit, 24 fr, softclamp kit, 24fr, straightshot kit, 23 fr, straight tip, straightshot kit, 23 fr, angled tip HEARTPORT, INC. K994243 05/05/2000
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