K-number	K991194
Device name	MODIFICATION TO ULTRA-SELECT GUIDEWIRE
Applicant	Microvena Corp.
Product code	DQX
Device class	Class II
Decision date	May 5, 1999
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ULTRA-SELECT GUIDEWIRE

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