K-number	K092298
Device name	MODIFICATION TO MODIFIED HD GUIDE CATHETER
Applicant	Concentric Medical, Inc.
Product code	DQY
Device class	Class II
Decision date	Nov 5, 2009
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO MODIFIED HD GUIDE CATHETER

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