K-number	K864316
Device name	TARGET THERAPEUTICS TAPER GUIDE WIRE
Applicant	Target Therapeutics
Product code	DQX
Device class	Class II
Decision date	Mar 20, 1987
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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TARGET THERAPEUTICS TAPER GUIDE WIRE

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