AO NON-CONTACT II TONOMETER

AO NON-CONTACT II TONOMETER is an FDA 510(k)-cleared medical device (K802419) manufactured by American Optical Corp.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 11, 1980. Regulation: 8.