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Medisurg , Ltd.
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FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300 is an FDA 510(k)-cleared medical device (K050933) manufactured by Medisurg , 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 December 8, 2005. Regulation: 8.