MODEL 5400 OPTOKINETIC STIMULATOR

MODEL 5400 OPTOKINETIC STIMULATOR is an FDA 510(k)-cleared medical device (K822917) manufactured by Life-Tech Intl., Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 31, 1982. Regulation: 8.