OSHER SURGICAL GONIO/POSTERIOR POLE LENS

OSHER SURGICAL GONIO/POSTERIOR POLE LENS is an FDA 510(k)-cleared medical device (K935302) manufactured by Ocular Instruments, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 31, 1994. Regulation: 8.