LASERMATIC COMBOLASER MODEL 5050

LASERMATIC COMBOLASER MODEL 5050 is an FDA 510(k)-cleared medical device (K895279) manufactured by Lasermatic OY. 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 7, 1989. Regulation: 8.