
Fiberoptic Medical Products, Inc.
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FIBEROPTIC LARYNGOSCOPE HANDLE is an FDA 510(k)-cleared medical device (K944686) manufactured by Fiberoptic Medical Products, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 3, 1994. Regulation: 8.

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