K-number	K863178
Device name	UMI STEERABLE TORQUE GUIDE WIRE
Applicant	Universal Medical Instrument Corp.
Product code	DQX
Device class	Class II
Decision date	Sep 19, 1986
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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UMI STEERABLE TORQUE GUIDE WIRE

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