K-number	K931327
Device name	PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE
Applicant	Peripheral Systems Group
Product code	DQX
Device class	Class II
Decision date	Jul 14, 1993
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE

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