BONASSE CONTACT LENS CASE

BONASSE CONTACT LENS CASE is an FDA 510(k)-cleared medical device (K991206) manufactured by Bonasse Ent. Co., Ltd.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 5, 2000. Regulation: 8.