STORZ FIBEROPTIC ENDO-ILLUMINATORS

STORZ FIBEROPTIC ENDO-ILLUMINATORS is an FDA 510(k)-cleared medical device (K896549) manufactured by Storz Instrument 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 February 14, 1990. Regulation: 8.