K-number	K102519
Device name	FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX
Applicant	Flexible Stenting Solutions, Inc.
Product code	FGE
Device class	Class II
Decision date	Nov 22, 2010
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX

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