K-number	K122581
Device name	MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254
Applicant	Concentric Medical, Inc.
Product code	DQY
Device class	Class II
Decision date	Nov 21, 2012
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254

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