K-number	K083343
Device name	HEADWAY 17 MICROCATHETER
Applicant	MicroVention, Inc.
Product code	DQY
Device class	Class II
Decision date	Dec 4, 2008
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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HEADWAY 17 MICROCATHETER

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