BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8

BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8 is an FDA 510(k)-cleared medical device (K924778) manufactured by R.H. Burton Co.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 4, 1993. Regulation: 8.