CATARACT LIQUEFRACTURE DEVICE

CATARACT LIQUEFRACTURE DEVICE is an FDA 510(k)-cleared medical device (K980292) manufactured by Alcon Laboratories. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 1998. Regulation: 8.