INTIMAX THROMBECTOMY CATHETER

INTIMAX THROMBECTOMY CATHETER is an FDA 510(k)-cleared medical device (K910372) manufactured by Applied Vascular Devices, 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 April 25, 1991. Regulation: 8.