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Dynarex Corp.
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DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B is an FDA 510(k)-cleared medical device (K012917) manufactured by Dynarex Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 27, 2001. Regulation: 8.

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