Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is an FDA 510(k)-cleared medical device (K183290) 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 February 24, 2019. Regulation: 8.