CYNOSURE ACCLAIM DERMATOLOGY LASER

CYNOSURE ACCLAIM DERMATOLOGY LASER is an FDA 510(k)-cleared medical device (K011828) manufactured by Cynosure, 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 September 6, 2001. Regulation: 8.