OPTILITE FIBEROPTIC DELIVERY SYSTEMS

OPTILITE FIBEROPTIC DELIVERY SYSTEMS is an FDA 510(k)-cleared medical device (K902871) manufactured by Xintec Corporation. 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 September 23, 1990. Regulation: 8.