C02 LASER MULTIPULSE

C02 LASER MULTIPULSE is an FDA 510(k)-cleared medical device (K002032) 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 10, 2000. Regulation: 8.