MENICON PROGENT REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES

MENICON PROGENT REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES is an FDA 510(k)-cleared medical device (K020930) manufactured by Menicon 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 May 1, 2002. Regulation: 8.