K-number	K221660
Device name	RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP
Applicant	Olympus Medical Systems Corp.
Product code	EOB
Device class	Class II
Decision date	Dec 28, 2022
Decision	Substantially Equivalent
Regulation	874.4760

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View the full FDA submission: accessdata.fda.gov

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RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP

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