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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: 11/24/2017
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directflow kit, 24 fr, softclamp kit, 24 heartport, inc. K994243 05/05/2000
quickdraw venous cannula heartport, inc. K981995 04/20/1999
directflow arterial cannula heartport, inc. K990772 03/23/1999
heartport endopulmonary vent catheter heartport, inc. K981009 09/04/1998
heartport direct aortic return cannula w heartport, inc. K974736 07/15/1998
heartport endoarterial return cannula heartport, inc. K971291 06/17/1997
heartport endovenous drainage cannula heartport, inc. K962835 02/10/1997
heartport endocoronary sinus cathetr heartport, inc. K964248 01/22/1997
heartport endopulmonary vent heartport, inc. K961245 06/18/1996
heartport endosinus catheter heartport, inc. K961270 06/18/1996