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Abbott Vascular, Inc.

FDA 510(k) & PMA Approved Devices — 19 products

Total Devices19
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K123067 PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILYDQX2013-01-29 View
510(k) K122573 HI-TORQUE COMMAND GUIDE WIRE FAMILYDQX2012-11-20 View
510(k) K102705 ARMADA 14 PTA CATHETERLIT2010-12-07 View
510(k) K101648 HI-TORQUE WINN GUIDE WIRE FAMILYDQX2010-07-08 View
510(k) K101011 HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSALDQX2010-05-24 View
510(k) K091825 HI-TORQUE PROGRESS GUIDE WIRE FAMILYDQX2009-09-25 View
510(k) K081417 FOXCROSS PTA CATHETERLIT2008-06-04 View
510(k) K080925 FOX PLUS PTA CATHETERLIT2008-04-28 View
510(k) K072460 HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II GUIDE WIREDQX2008-04-11 View
510(k) K063481 MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEMFGE2007-09-14 View
510(k) K062554 STARCLOSE HEX-HUB DILATORDRE2007-02-06 View
510(k) K060902 STARCLOSE INTRODUCER SET MODEL- 1002DYB2006-07-07 View
510(k) K032929 MODIFICATION TO:XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 14819, 14820, 14821, 14822, 14822FGE2003-10-22 View
510(k) K031331 WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEMFGE2003-08-12 View
510(k) K021062 CHITO-SEALQSY2002-08-23 View
510(k) K014118 MODIFICATION TO SUPERCROSS CATHETERDQY2002-01-11 View
510(k) K013683 MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICEGAW2001-12-06 View
510(k) K001856 SUPERCROSS CATHETERDQY2001-03-07 View
510(k) K001703 PERCLOSE VASCULAR SUTURE DELIVERY DEVICEGAW2000-10-03 View
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