
Deka Research & Development Corp.
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DEKA TAC DEVICE is an FDA 510(k)-cleared medical device (K093915) manufactured by Deka Research & Development Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 22, 2011. Regulation: 8.

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