Bashir Plus Endovascular Catheter

Bashir Plus Endovascular Catheter is an FDA 510(k)-cleared medical device (K193071) manufactured by Thrombolex, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 2019. Regulation: 8.