K-number	K032530
Device name	MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM
Applicant	Guidant Corporation
Product code	FGE
Device class	Class II
Decision date	Oct 23, 2003
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM

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