K-number	K051919
Device name	MODIFICATION TO: USGI SHAPELOCK ENDOSCOPIC GUIDE
Applicant	Usgi Medical
Product code	FED
Device class	Class II
Decision date	Jul 26, 2005
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO: USGI SHAPELOCK ENDOSCOPIC GUIDE

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