K-number	K003336
Device name	MODIFICATION TO S.M.A.R.T NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Applicant	Cordis Corp.
Product code	FGE
Device class	Class II
Decision date	Nov 22, 2000
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO S.M.A.R.T NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

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