K-number	K180341
Device name	FUJIFILM 600 Series Endoscope EG-600WR v2
Applicant	Fujifilm Corporation
Product code	FDS
Device class	Class II
Decision date	Aug 3, 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 600 Series Endoscope EG-600WR v2

Everything you need for a 510(k) submission. Nothing you don't.