K-number	K024058
Device name	MODIFICATION TO CARDEON AEGIS CATHETER
Applicant	Cardeon Corp.
Product code	DWF
Device class	Class II
Decision date	Dec 30, 2002
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO CARDEON AEGIS CATHETER

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