K-number	K140438
Device name	MICRO GUIDE CATHETER ELITE
Applicant	Cordis Corp., A Johnson & Johnson Co.
Product code	PDU
Device class	Class II
Decision date	Nov 14, 2014
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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MICRO GUIDE CATHETER ELITE

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