K-number	K024048
Device name	MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM
Applicant	Boston Scientific Scimed, Inc.
Product code	FGE
Device class	Class II
Decision date	Jan 6, 2003
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM

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