DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES

DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES is an FDA 510(k)-cleared medical device (K934309) manufactured by U.S. Toy Co., Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 1, 1993. Regulation: 8.