K-number	K092221
Device name	COLONIC SPLINTING OVERTUBE, MODEL 00711145
Applicant	United States Endoscopy Group, Inc.
Product code	FED
Device class	Class II
Decision date	Oct 20, 2009
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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COLONIC SPLINTING OVERTUBE, MODEL 00711145

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