LANDERS INDIRECT VITRECTOMY LENS

LANDERS INDIRECT VITRECTOMY LENS is an FDA 510(k)-cleared medical device (K864418) manufactured by Ocular Instruments, 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 27, 1986. Regulation: 8.