MODEL 2000 INTRAOPERATIVE CORNEASCOPE

MODEL 2000 INTRAOPERATIVE CORNEASCOPE is an FDA 510(k)-cleared medical device (K901009) manufactured by Kera Corp.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 29, 1990. Regulation: 8.