COOPERVISION ACAP POWER DRIVE ULTRASONIC ANTERIOR

COOPERVISION ACAP POWER DRIVE ULTRASONIC ANTERIOR is an FDA 510(k)-cleared medical device (K854375) 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 December 26, 1985. Regulation: 8.