K-number	K880762
Device name	TAPER FLEX-TIP STEERABLE GUIDEWIRE
Applicant	Target Therapeutics
Product code	DQX
Device class	Class II
Decision date	Aug 19, 1988
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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TAPER FLEX-TIP STEERABLE GUIDEWIRE

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