K-number	K100081
Device name	ENTEROSCOPY OVERTUBE, MODEL 00712140
Applicant	United States Endoscopy Group, Inc.
Product code	FED
Device class	Class II
Decision date	Apr 12, 2010
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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ENTEROSCOPY OVERTUBE, MODEL 00712140

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