K-number	K001033
Device name	AGILITY STEERABLE GUIDEWIRE
Applicant	Cordis Neurovascular, Inc.
Product code	DQX
Device class	Class II
Decision date	Apr 14, 2000
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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AGILITY STEERABLE GUIDEWIRE

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