
Bruel & Kjaer Industri A/S
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RHINO-LARYNX STROBOSCOPE TYPE 4914 is an FDA 510(k)-cleared medical device (K842090) manufactured by Bruel & Kjaer Industri A/S. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 17, 1984. Regulation: 8.

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