SHARPLAN 723 CO2 LASER SURGICAL SYSTEM

SHARPLAN 723 CO2 LASER SURGICAL SYSTEM is an FDA 510(k)-cleared medical device (K801624) 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 August 19, 1980. Regulation: 8.