K-number	K832650
Device name	UPSHER FIBERBRITE LARYNGOSCOPE
Applicant	Michael S. Upsher
Product code	CCW
Device class	Class I
Decision date	Sep 12, 1983
Decision	Substantially Equivalent
Regulation	868.5540

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View the full FDA submission: accessdata.fda.gov

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UPSHER FIBERBRITE LARYNGOSCOPE

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