K-number	K162836
Device name	FUJIFILM Surgical System
Applicant	Fujifilm New Development U.S.A., Inc.
Product code	GCJ
Device class	Class II
Decision date	Mar 13, 2017
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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FUJIFILM Surgical System

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