K-number	K983791
Device name	PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA
Applicant	Edwards Lifesciences Research Medical
Product code	DWF
Device class	Class II
Decision date	Jun 11, 1999
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA

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