K-number	K962759
Device name	4F NYLEX ANGIOGRAPHIC CATHETER
Applicant	Cordis Corp.
Product code	DQO
Device class	Class II
Decision date	Oct 10, 1996
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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4F NYLEX ANGIOGRAPHIC CATHETER

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