QRK 100, QUALITATIVE RING KERATOSCOPE

QRK 100, QUALITATIVE RING KERATOSCOPE is an FDA 510(k)-cleared medical device (K882902) manufactured by Technitex, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 3, 1988. Regulation: 8.