OMNIGUIDE ZERO FLOW ZF-T 150 WAVEGUIDE FIBER

OMNIGUIDE ZERO FLOW ZF-T 150 WAVEGUIDE FIBER is an FDA 510(k)-cleared medical device (K063141) 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 November 28, 2006. Regulation: 8.