CYNOSURE PHOTOGENICA P PIGMENTED LESION LASER

CYNOSURE PHOTOGENICA P PIGMENTED LESION LASER is an FDA 510(k)-cleared medical device (K921841) 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 August 3, 1992. Regulation: 8.