K-number	K012993
Device name	MODIFICATION TO PRECISE NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Applicant	Cordis Corp.
Product code	FGE
Device class	Class II
Decision date	Oct 5, 2001
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO PRECISE NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

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