MCL 29 DERMABLATE ERBIUM LASER SYSTEM

MCL 29 DERMABLATE ERBIUM LASER SYSTEM is an FDA 510(k)-cleared medical device (K964128) 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 March 16, 1997. Regulation: 8.