K-number	K092303
Device name	MERIT LAUREATE HYDROPHILIC GUIDE WIRE
Applicant	Merit Medical Systems, Inc.
Product code	DQX
Device class	Class II
Decision date	Oct 27, 2009
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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MERIT LAUREATE HYDROPHILIC GUIDE WIRE

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