K-number	K112381
Device name	HI TORQUE CONNECT GUIDEWIRE
Applicant	Lake Region Medical
Product code	DQX
Device class	Class II
Decision date	Nov 3, 2011
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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HI TORQUE CONNECT GUIDEWIRE

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