ITEM #272 MAGNIF-EYES CONTACT LENS CASE

ITEM #272 MAGNIF-EYES CONTACT LENS CASE is an FDA 510(k)-cleared medical device (K900778) manufactured by Magnivision, 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 March 29, 1990. Regulation: 8.