DAYTONA ICG (P200TICG)

DAYTONA ICG (P200TICG) is an FDA 510(k)-cleared medical device (K134039) manufactured by Optos Plc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 10, 2014. Regulation: 8.