CERALAS G15 532NM FREQUENCY DOUBLED ND:YAG LASER, MODEL G1-G15

CERALAS G15 532NM FREQUENCY DOUBLED ND:YAG LASER, MODEL G1-G15 is an FDA 510(k)-cleared medical device (K002296) manufactured by Ceram Optec, Inc.. 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 October 1, 2000. Regulation: 8.