K-number	K011039
Device name	OMNILINK .018 BILIARY STENT SYSTEM
Applicant	Guidant Corp.
Product code	FGE
Device class	Class II
Decision date	May 8, 2001
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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OMNILINK .018 BILIARY STENT SYSTEM

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