K-number	K023121
Device name	LIFESTENT BILIARY ENDOPROSTHESIS
Applicant	Orbus Medical Technologies
Product code	FGE
Device class	Class II
Decision date	Mar 10, 2003
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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LIFESTENT BILIARY ENDOPROSTHESIS

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