MODEL 1000 OPHTHALMIC LASER SYSTEM

MODEL 1000 OPHTHALMIC LASER SYSTEM is an FDA 510(k)-cleared medical device (K862987) 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 September 23, 1986. Regulation: 8.