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 6 of 6 Results
ProductCode: DWF Applicant: C.R. BARD, INC. Decision Date To: 05/16/2022
Results per Page
New Search  
Export all 6 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]
amendment william harvey h-4300 cardiopulmonary su C.R. BARD, INC. K851323 08/12/1985
bard extracorporeal circulation cannulae C.R. BARD, INC. K902277 08/14/1990
bard william harvey aortic arch canulae C.R. BARD, INC. K923483 03/22/1993
bard william harvey aortic root cardioplegia cannu C.R. BARD, INC. K930593 05/06/1993
bard(r) william harvey(r) arterial straigh cannula C.R. BARD, INC. K930620 05/07/1993
bard william harvey two stage cannula C.R. BARD, INC. K930684 05/11/1993
-
-