
M. Imonti and Associates Inc.,
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PRO-VIT is an FDA 510(k)-cleared medical device (K950799) manufactured by M. Imonti and Associates Inc.,. 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 27, 1995. Regulation: 8.

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