
Starkey Laboratories, Inc.
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STARKEY TRILOGY II PROGRAMMABLE HEARING AID is an FDA 510(k)-cleared medical device (K933113) manufactured by Starkey Laboratories, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 26, 1993. Regulation: 8.

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