MENTOR ANTERIOR SEGMENT VITRECTOR

MENTOR ANTERIOR SEGMENT VITRECTOR is an FDA 510(k)-cleared medical device (K890595) manufactured by Mentor O & O, 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 April 16, 1989. Regulation: 8.