K-number	K181763
Device name	FUJIFILM Ultrasonic Endoscope
Applicant	Fujifilm Corporation
Product code	FDS
Device class	Class II
Decision date	Jul 27, 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 Ultrasonic Endoscope

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