TUTTIFRUTTI (NON-PRES. SUNGLASSES)

TUTTIFRUTTI (NON-PRES. SUNGLASSES) is an FDA 510(k)-cleared medical device (K801922) manufactured by Safety Plastics of New York. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 11, 1980. Regulation: 8.