STORZ FIBEROPTIC REVERSE CUTTING KNIFE

STORZ FIBEROPTIC REVERSE CUTTING KNIFE is an FDA 510(k)-cleared medical device (K933984) manufactured by Storz Instrument Co.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 24, 1994. Regulation: 8.