LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM

LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM is an FDA 510(k)-cleared medical device (K982940) manufactured by Star Medical Technologies, Inc.. 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 7, 1999. Regulation: 8.