COOPER VISION I/A SYSTEM III MODEL 1500

COOPER VISION I/A SYSTEM III MODEL 1500 is an FDA 510(k)-cleared medical device (K822220) manufactured by CooperVision, 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 October 5, 1982. Regulation: 8.