K-number	K895903
Device name	IVT 0.014 GUIDE WIRE
Applicant	Intensive Technology, Inc.
Product code	DQX
Device class	Class II
Decision date	Jan 4, 1990
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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IVT 0.014 GUIDE WIRE

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