LASER PERIPHERALS INC. BARE FIBER

LASER PERIPHERALS INC. BARE FIBER is an FDA 510(k)-cleared medical device (K961516) manufactured by Laser Peripherals, 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 June 26, 1996. Regulation: 8.