ADD'L USE OF THE KTP/YAG SURGICAL LASER

ADD'L USE OF THE KTP/YAG SURGICAL LASER is an FDA 510(k)-cleared medical device (K902058) manufactured by Laserscope. 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 28, 1990. Regulation: 8.