OMNIGUIDE ZERO FLOW ZF-T WAVEGUIDE FIBER

OMNIGUIDE ZERO FLOW ZF-T WAVEGUIDE FIBER is an FDA 510(k)-cleared medical device (K070071) 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 24, 2007. Regulation: 8.