
Mountain Precision Mfg. Ltd. Co.
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NU-VOIS BATTERY POWERED ARTIFICIAL LARYNX is an FDA 510(k)-cleared medical device (K934483) manufactured by Mountain Precision Mfg. Ltd. Co.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 15, 1994. Regulation: 8.

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