K-number	K094062
Device name	PERCU-PRO GUIDEWIRE
Applicant	Cardiosolutions, Inc.
Product code	DQX
Device class	Class II
Decision date	Sep 27, 2010
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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PERCU-PRO GUIDEWIRE

Everything you need for a 510(k) submission. Nothing you don't.