CYNOSURE PHOTOGENICA ER

CYNOSURE PHOTOGENICA ER is an FDA 510(k)-cleared medical device (K012790) 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 November 15, 2001. Regulation: 8.