K-number	K913842
Device name	CORDIS RIGHT-ANGLE CATHETER GUIDE
Applicant	Cordis Corp.
Product code	JXG
Device class	Class II
Decision date	Feb 19, 1992
Decision	Substantially Equivalent
Regulation	882.5550

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View the full FDA submission: accessdata.fda.gov

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CORDIS RIGHT-ANGLE CATHETER GUIDE

Everything you need for a 510(k) submission. Nothing you don't.