K-number	K991898
Device name	ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE
Applicant	Microvena Corp.
Product code	DQX
Device class	Class II
Decision date	Jun 16, 1999
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE

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