K-number	K130792
Device name	LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEM
Applicant	C.R. Bard, Inc.
Product code	FGE
Device class	Class II
Decision date	Aug 30, 2013
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEM

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