
Danavox, Inc.
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BEHINDTHEEAR HEAR. AID MOD. 793U,M,UH,MH is an FDA 510(k)-cleared medical device (K792334) manufactured by Danavox, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 17, 1979. Regulation: 8.

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