Bashir S-B Endovascular Catheter, Ref. No. 7101

Bashir S-B Endovascular Catheter, Ref. No. 7101 is an FDA 510(k)-cleared medical device (K192598) 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 October 17, 2019. Regulation: 8.