K-number	K173650
Device name	AquaShield System CO2- Fujifilm
Applicant	United States Endoscopy Group, Inc.
Product code	FEQ
Device class	Class II
Decision date	Jan 5, 2018
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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AquaShield System CO2- Fujifilm

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