K-number	K002212
Device name	MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608
Applicant	Micro Therapeutics, Inc.
Product code	DQX
Device class	Class II
Decision date	Aug 3, 2000
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608

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