FIBEROPTIC LIGHT SOURCE, FOI-1A

FIBEROPTIC LIGHT SOURCE, FOI-1A is an FDA 510(k)-cleared medical device (K896384) manufactured by Jedmed Instrument Co.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 22, 1990. Regulation: 8.