Abbott Vascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Abbott Vascular - FDA 510(k) Cleared Devices
Recent clearances: NC TREK NEO Coronary Dilatation Catheter, Viatrac 14 Plus Peripheral Dilatation Catheter, HI-TORQUE PROCEED Guide Wire Family
30
Total
30
Cleared
0
Denied
Abbott Vascular has 30 FDA 510(k) cleared cardiovascular devices. Based in S,Mta Clara, US.
Last cleared in 2022. Active since 2009.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Abbott Vascular
30 devices
Cleared
Jun 30, 2022
NC TREK NEO Coronary Dilatation Catheter
Cardiovascular
118d
Cleared
May 05, 2022
Viatrac 14 Plus Peripheral Dilatation Catheter
Cardiovascular
24d
Cleared
Jul 30, 2020
HI-TORQUE PROCEED Guide Wire Family
Cardiovascular
28d
Cleared
Apr 08, 2020
HI-TORQUE Steelcore Bare Guide Wire
Cardiovascular
77d
Cleared
Dec 11, 2019
HI-TORQUE InfilTrac Guide Wire Family
Cardiovascular
29d
Cleared
Jul 25, 2019
Emboshield NAV6 Embolic Protection System, Barewire Filter Delivery Wires
Cardiovascular
85d
Cleared
Aug 24, 2018
NC TREK™ RX Coronary Dilatation Catheter
Cardiovascular
231d
Cleared
Jan 12, 2018
HI-TORQUE TurnTrac Guide Wire Family
Cardiovascular
29d
Cleared
Sep 06, 2017
Steerable Guide Catheter
Cardiovascular
29d
Cleared
Aug 25, 2017
Hi-Torque Command 18 Guide Wire
Cardiovascular
46d
Cleared
Aug 07, 2016
Steerable Guide Catheter
Cardiovascular
19d
Cleared
Nov 20, 2015
RX ACCUNET Embolic Protection System
Cardiovascular
25d