LASERSCOPE'S MICROSPOT DERMASTAT

LASERSCOPE'S MICROSPOT DERMASTAT is an FDA 510(k)-cleared medical device (K914918) 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 July 23, 1992. Regulation: 8.