LEMAITRE OCCLUSION CATHETER

LEMAITRE OCCLUSION CATHETER is an FDA 510(k)-cleared medical device (K992942) manufactured by Vascutech, 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 12, 2000. Regulation: 8.