K-number	K081021
Device name	KINETIX GUIDEWIRE, PLUS GUIDEWIRE
Applicant	Boston Scientific Corp
Product code	DQX
Device class	Class II
Decision date	Aug 8, 2008
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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KINETIX GUIDEWIRE, PLUS GUIDEWIRE

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