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Becton, Dickinson & CO
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BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME is an FDA 510(k)-cleared medical device (K022637) manufactured by Becton, Dickinson & CO. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 15, 2002. Regulation: 8.