ANDIODYNAMICS, INC. ELVS PROCEDURE KIT

ANDIODYNAMICS, INC. ELVS PROCEDURE KIT is an FDA 510(k)-cleared medical device (K031233) 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 June 17, 2003. Regulation: 8.