K-number	K993392
Device name	BARD MEMOTHERM FLEXX BILIARY STENT
Applicant	C.R. Bard, Inc.
Product code	FGE
Device class	Class II
Decision date	Jan 6, 2000
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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BARD MEMOTHERM FLEXX BILIARY STENT

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