K-number	K221551
Device name	FUJIFILM Endoscope Model EI-740D/S
Applicant	Fujifilm Corporaton
Product code	FDS
Device class	Class II
Decision date	Jan 27, 2023
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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FUJIFILM Endoscope Model EI-740D/S

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