MULTIPULSE CO2 LASER

MULTIPULSE CO2 LASER is an FDA 510(k)-cleared medical device (K983215) manufactured by Aesculap-Meditec GmbH. 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 December 3, 1998. Regulation: 8.