FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLE

FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLE is an FDA 510(k)-cleared medical device (K901035) manufactured by Cuda Products Co.. 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 April 22, 1990. Regulation: 8.