K-number	K210162
Device name	Endoscope Model EI-740D/S
Applicant	Fujifilm Corporation
Product code	FDS
Device class	Class II
Decision date	Apr 9, 2021
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Endoscope Model EI-740D/S

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