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Escalon Medical Corp.
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MEGAVISION CPX, MEGAVISION FA, MODEL I AND II is an FDA 510(k)-cleared medical device (K002920) manufactured by Escalon Medical Corp.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 2000. Regulation: 8.