K-number	K032025
Device name	SENTINOL NITINOL BILLARY STENT SYSTEM
Applicant	Boston Scientific Corp
Product code	FGE
Device class	Class II
Decision date	Sep 25, 2003
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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SENTINOL NITINOL BILLARY STENT SYSTEM

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