
Telesonic, Inc.
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TELESONIC ARCON & SOUNDEX ASP 101 is an FDA 510(k)-cleared medical device (K802597) manufactured by Telesonic, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 11, 1980. Regulation: 8.

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