K-number	K923607
Device name	RADIFOCUS GUIDE WIRE M
Applicant	Terumo Medical Corp.
Product code	KOD
Device class	Class II
Decision date	Oct 2, 1992
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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RADIFOCUS GUIDE WIRE M

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