K-number	K001371
Device name	CARDEON ASCENDING BALLOON CANNULA (ABC)
Applicant	Cardeon Corp.
Product code	DWF
Device class	Class II
Decision date	Jul 7, 2000
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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CARDEON ASCENDING BALLOON CANNULA (ABC)

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