CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPS

CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPS is an FDA 510(k)-cleared medical device (K014048) manufactured by Clinicon Corp.. 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 February 10, 2002. Regulation: 8.