MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM

MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM is an FDA 510(k)-cleared medical device (K901340) manufactured by Klinger Medical. 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 June 25, 1990. Regulation: 8.