LASERSYSTEM BEAUTYSTAR 532

LASERSYSTEM BEAUTYSTAR 532 is an FDA 510(k)-cleared medical device (K021975) manufactured by Asclepion-Meditec AG. 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 12, 2002. Regulation: 8.