ARISTAR EYEWEAR, ESPRIT EYEWEAR

ARISTAR EYEWEAR, ESPRIT EYEWEAR is an FDA 510(k)-cleared medical device (K945123) manufactured by Aristar Inc. U.S.A.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 21, 1994. Regulation: 8.