BARE-FIBER ENDOILLUMINATOR

BARE-FIBER ENDOILLUMINATOR is an FDA 510(k)-cleared medical device (K933208) manufactured by Surgical Technologies, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 13, 1993. Regulation: 8.