OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDE

OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDE is an FDA 510(k)-cleared medical device (K853598) manufactured by Myocure, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 3, 1985. Regulation: 8.