NIDEK KM-800 AUTO KERATOMETER

NIDEK KM-800 AUTO KERATOMETER is an FDA 510(k)-cleared medical device (K861063) manufactured by Nidek, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 3, 1986. Regulation: 8.