HORIZON/WESTHIN 55-G

HORIZON/WESTHIN 55-G is an FDA 510(k)-cleared medical device (K962121) manufactured by Westcon Contact Lens Co., 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 August 25, 1996. Regulation: 8.