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Abbott Vascular, Inc.

20 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Hi-Torque JET Guide Wire Family (K142415)Abbott Vascular, Inc.2014-12-19
PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILY (K123067)Abbott Vascular, Inc.2013-01-29
HI-TORQUE COMMAND GUIDE WIRE FAMILY (K122573)Abbott Vascular, Inc.2012-11-20
ARMADA 14 PTA CATHETER (K102705)Abbott Vascular, Inc.2010-12-07
HI-TORQUE WINN GUIDE WIRE FAMILY (K101648)Abbott Vascular, Inc.2010-07-08
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL (K101011)Abbott Vascular, Inc.2010-05-24
HI-TORQUE PROGRESS GUIDE WIRE FAMILY (K091825)Abbott Vascular, Inc.2009-09-25
FOXCROSS PTA CATHETER (K081417)Abbott Vascular, Inc.2008-06-04
FOX PLUS PTA CATHETER (K080925)Abbott Vascular, Inc.2008-04-28
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II GUIDE WIRE (K072460)Abbott Vascular, Inc.2008-04-11
MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEM (K063481)Abbott Vascular, Inc.2007-09-14
STARCLOSE HEX-HUB DILATOR (K062554)Abbott Vascular, Inc.2007-02-06
STARCLOSE INTRODUCER SET MODEL- 1002 (K060902)Abbott Vascular, Inc.2006-07-07
MODIFICATION TO:XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 14819, 14820, 14821, 14822, 14822 (K032929)Abbott Vascular, Inc.2003-10-22
WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM (K031331)Abbott Vascular, Inc.2003-08-12
CHITO-SEAL (K021062)Abbott Vascular, Inc.2002-08-23
MODIFICATION TO SUPERCROSS CATHETER (K014118)Abbott Vascular, Inc.2002-01-11
MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICE (K013683)Abbott Vascular, Inc.2001-12-06
SUPERCROSS CATHETER (K001856)Abbott Vascular, Inc.2001-03-07
PERCLOSE VASCULAR SUTURE DELIVERY DEVICE (K001703)Abbott Vascular, Inc.2000-10-03

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Every clearance here is in the API, with alerts when new ones post.