CYNOSURE APOGEE-TKS II DERMATOLOGICAL LASER

CYNOSURE APOGEE-TKS II DERMATOLOGICAL LASER is an FDA 510(k)-cleared medical device (K031488) 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 June 3, 2003. Regulation: 8.