KTP/532 AND KTP/YAG

KTP/532 AND KTP/YAG is an FDA 510(k)-cleared medical device (K913758) 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 November 19, 1991. Regulation: 8.