OPTEC 1000 DMV VISION TESTER MODIFY

OPTEC 1000 DMV VISION TESTER MODIFY is an FDA 510(k)-cleared medical device (K875237) manufactured by Stereo Optical Co., Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 16, 1988. Regulation: 8.