K-number	K080364
Device name	FINDRWIRZ GUIDE WIRE SYSTEM
Applicant	Sentreheart, Inc.
Product code	DQX
Device class	Class II
Decision date	Aug 11, 2008
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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FINDRWIRZ GUIDE WIRE SYSTEM

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