K-number	K930961
Device name	CATHETER GUIDEWIRE (PERIPHERAL USE)
Applicant	Target Therapeutics
Product code	DQX
Device class	Class II
Decision date	May 26, 1993
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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CATHETER GUIDEWIRE (PERIPHERAL USE)

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