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Edwards Lifesciences Research Medical

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K073559	18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA II	DQR	2008-01-31	View
510(k)	K062429	MODIFICATION TO EMBOL-X INTRA-AORTIC FILTER: X-SMALL, SMALL, MEDIUM, LARGE, X-LARGE WITH HEPARIN COATED MESH	DTM	2006-09-27	View
510(k)	K990396	T-ANASTAFLO	DWF	1999-10-01	View
510(k)	K991170	RETROGRADE CARDIOPLEGIA CANNULA WITH DURAFLO TREATMENT, MODEL DII-RC-014	DWF	1999-07-02	View
510(k)	K983791	PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA	DWF	1999-06-11	View
510(k)	K974259	VENOUS FLEX II PERIPHERAL AND INTRA-OPERATIVE ACCESS VENOUS RETURN CANNULAE	DWF	1998-12-01	View

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