K-number	K223469
Device name	WallFlex Biliary RX Stent System
Applicant	Boston Scientific Corporation
Product code	FGE
Device class	Class II
Decision date	Jun 15, 2023
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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WallFlex Biliary RX Stent System

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WallFlex Biliary RX Stent System