CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE

CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE is an FDA 510(k)-cleared medical device (K934337) 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 November 17, 1993. Regulation: 8.