K-number	K100351
Device name	NEUROSCOUT STEERABLE GUIDEWIRE
Applicant	Codman & Shurtleff, Inc.
Product code	DQX
Device class	Class II
Decision date	Mar 16, 2010
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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NEUROSCOUT STEERABLE GUIDEWIRE

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