K-number	K120123
Device name	AQUASHIELD CO2 SYSTEM
Applicant	United States Endoscopy Group, Inc.
Product code	FEQ
Device class	Class II
Decision date	Mar 28, 2012
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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AQUASHIELD CO2 SYSTEM

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