Abbott Vascular, Inc. is one of 12964 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Abbott Vascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Hi-Torque JET Guide Wire Family, PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILY, HI-TORQUE COMMAND GUIDE WIRE FAMILY
20
Total
17
Cleared
0
Denied
Abbott Vascular, Inc. has 17 FDA 510(k) cleared cardiovascular devices. Based in Redwood, US.
Historical record: 17 cleared submissions from 2000 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Abbott Vascular, Inc.
20 devices
Cleared
Dec 19, 2014
Hi-Torque JET Guide Wire Family
Cardiovascular
113d
Cleared
CT
Jan 29, 2013
PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILY
Cardiovascular
120d
Cleared
Nov 20, 2012
HI-TORQUE COMMAND GUIDE WIRE FAMILY
Cardiovascular
89d
Cleared
Dec 07, 2010
ARMADA 14 PTA CATHETER
Cardiovascular
78d
Cleared
Jul 08, 2010
HI-TORQUE WINN GUIDE WIRE FAMILY
Cardiovascular
27d
Cleared
May 24, 2010
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL
Cardiovascular
42d
Cleared
Sep 25, 2009
HI-TORQUE PROGRESS GUIDE WIRE FAMILY
Cardiovascular
98d
Cleared
Jun 04, 2008
FOXCROSS PTA CATHETER
Cardiovascular
15d
Cleared
Apr 28, 2008
FOX PLUS PTA CATHETER
Cardiovascular
26d
Cleared
Apr 11, 2008
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II GUIDE WIRE
Cardiovascular
224d
Cleared
Sep 14, 2007
MODIFICATION TO RX HERCULINK ELITE BILIARY STENT SYSTEM
Gastroenterology & Urology
301d
Cleared
Feb 06, 2007
STARCLOSE HEX-HUB DILATOR
Cardiovascular
160d