AUTOMATED INTRAOCULAR SCISSORS

AUTOMATED INTRAOCULAR SCISSORS is an FDA 510(k)-cleared medical device (K842471) manufactured by Medical Instrument Development Laboratories, 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 November 20, 1984. Regulation: 8.