ANGIODYNAMICS, INC. 600UM FIBER AND VENACURE PROCEDURE KIT

ANGIODYNAMICS, INC. 600UM FIBER AND VENACURE PROCEDURE KIT is an FDA 510(k)-cleared medical device (K070378) 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 March 8, 2007. Regulation: 8.