LEMAITRE 8F OCCLUSION CATHETER

LEMAITRE 8F OCCLUSION CATHETER is an FDA 510(k)-cleared medical device (K132022) manufactured by LeMaitre Vascular, 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 November 5, 2013. Regulation: 8.