
Richards Medical Co., Inc.
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OMNI ITC TYPE HEARING AID MODEL U-IMPULSE SP is an FDA 510(k)-cleared medical device (K880286) manufactured by Richards Medical Co., Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 22, 1988. Regulation: 8.

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