DIGILAB 350 THE KRAKAU PERIMETER

DIGILAB 350 THE KRAKAU PERIMETER is an FDA 510(k)-cleared medical device (K832175) manufactured by Bio-Rad. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 15, 1983. Regulation: 8.