MODEL MC 1100 SURGICAL YAG LASER

MODEL MC 1100 SURGICAL YAG LASER is an FDA 510(k)-cleared medical device (K903943) manufactured by Klinger Micro-Controle Group. 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 November 20, 1990. Regulation: 8.