ANGIODYNAMICS, INC. VENACURE NEVERTOUCH DIRECT PROCEDURE KIT

ANGIODYNAMICS, INC. VENACURE NEVERTOUCH DIRECT PROCEDURE KIT is an FDA 510(k)-cleared medical device (K112600) manufactured by AngioDynamics, 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 January 29, 2012. Regulation: 8.