Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
1 to 10 of 11 Results
ProductCode: DWF Applicant: HEARTPORT, INC Decision Date To: 04/16/2014
 
 1 
 2 
 
Results per Page
New Search  
Export all 11 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
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
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 with introducer 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
-
-