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C.S.O. S.R.L.
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F 900 is an FDA 510(k)-cleared medical device (K022054) manufactured by C.S.O. S.R.L.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 2002. Regulation: 8.