FEATHERLITE DIODE LASER

FEATHERLITE DIODE LASER is an FDA 510(k)-cleared medical device (K980142) manufactured by Laserlite, LLC. 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 2, 1998. Regulation: 8.