K-number	K882804
Device name	0.014 PERIPHERAL GUIDE WIRE
Applicant	Intensive Technology, Inc.
Product code	DQX
Device class	Class II
Decision date	Oct 28, 1988
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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0.014 PERIPHERAL GUIDE WIRE

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