SHARPLAN 720 CO2 SURGICAL LASER

SHARPLAN 720 CO2 SURGICAL LASER is an FDA 510(k)-cleared medical device (K820101) manufactured by Laser Industries , Ltd.. 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 February 23, 1982. Regulation: 8.