ENDOVASCULAR LAER VEIN SYSTEM KIT

ENDOVASCULAR LAER VEIN SYSTEM KIT is an FDA 510(k)-cleared medical device (K101712) manufactured by Biolitec, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 26, 2010. Regulation: 8.