K-number	K992319
Device name	RX MEGALINK SDS BILIARY STENT SYSTEM, OTW MEGALINK SDS BILIARY STENT SYSTEM
Applicant	Guidant Corp.
Product code	FGE
Device class	Class II
Decision date	Oct 8, 1999
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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RX MEGALINK SDS BILIARY STENT SYSTEM, OTW MEGALINK SDS BILIARY STENT SYSTEM

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