K-number	K910931
Device name	BILIARY BALLOON DILATATION CATHETER
Applicant	Boston Scientific Corp
Product code	FGE
Device class	Class II
Decision date	Apr 2, 1991
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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BILIARY BALLOON DILATATION CATHETER

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