K-number	K023870
Device name	FLEXIMA BILIARY CATHETER
Applicant	Boston Scientific/Medi-Tech
Product code	FGE
Device class	Class II
Decision date	Dec 20, 2002
Decision	Substantially Equivalent
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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FLEXIMA BILIARY CATHETER

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