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 10 Results
ProductCode: LIT Applicant: Abbott Vascular Decision Date To: 04/19/2024
Results per Page
New Search  
Export all 10 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]
viatrac 14 plus peripheral dilatation catheter Abbott Vascular K221057 05/05/2022
armada 18 pta catheter ABBOTT VASCULAR K151317 07/06/2015
armada 14xxt pta catheter Abbott Vascular K121352 08/15/2012
armada 35/35ll pta catheter Abbott Vascular K111899 10/03/2011
armada 14 pta catheter ABBOTT VASCULAR INC. K102705 12/07/2010
fox sv pta catheter Abbott Vascular K092286 08/27/2009
foxcross pta catheter ABBOTT VASCULAR INC. K081417 06/04/2008
fox plus pta catheter ABBOTT VASCULAR INC. K080925 04/28/2008
modification to: fox plus pta catheter ABBOTT VASCULAR-VASCULAR SOLUTIONS K080264 03/26/2008
viatrac 14 plus peripheral dilation catheter ABBOTT VASCULAR-VASCULAR SOLUTIONS K072798 01/31/2008
-
-