
Welch Allyn, Inc.
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OTOSCOPE/ILLUMINATOR, MODEL #21100 is an FDA 510(k)-cleared medical device (K770769) manufactured by Welch Allyn, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 28, 1977. Regulation: 8.

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