LASER PERIPHERALS INC. SCATTERFREE FIBER

LASER PERIPHERALS INC. SCATTERFREE FIBER is an FDA 510(k)-cleared medical device (K961079) 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 May 21, 1996. Regulation: 8.