MENICON NECT CONTACT LENS CASE

MENICON NECT CONTACT LENS CASE is an FDA 510(k)-cleared medical device (K131875) manufactured by Foresight Regulatory Strategies. 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 5, 2013. Regulation: 8.