
Laserscope
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KTP/532 SURGICAL LASER SYSTEM W/KTP/YAG MODULE is an FDA 510(k)-cleared medical device (K895945) 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 April 8, 1990. Regulation: 8.