POMERANTZEFF EQUATOR PLUS CAMERA

POMERANTZEFF EQUATOR PLUS CAMERA is an FDA 510(k)-cleared medical device (K770888) manufactured by Medical Instrument Research Assoc., Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 2, 1977. Regulation: 8.