K-number	K010579
Device name	STENT SUPPORT GUIDE CATHETER
Applicant	Medtronic Vascular
Product code	DQY
Device class	Class II
Decision date	Nov 21, 2001
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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STENT SUPPORT GUIDE CATHETER

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