MARK III WAVEGUIDE FIBER WITH LOW PROFILE TIP

MARK III WAVEGUIDE FIBER WITH LOW PROFILE TIP is an FDA 510(k)-cleared medical device (K073313) manufactured by Omniguide, 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 January 1, 2008. Regulation: 8.