K-number	K182051
Device name	FUJIFILM Duodenoscope Model
Applicant	Fujifilm Corporation
Product code	FDT
Device class	Class II
Decision date	Oct 2, 2018
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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FUJIFILM Duodenoscope Model

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