Edwards Lifesciences Research Medical
Edwards Lifesciences Research Medical holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2008.
Top product codes for Edwards Lifesciences Research Medical
Recent clearances by Edwards Lifesciences Research Medical
- K073559 — 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA II
- K062429 — MODIFICATION TO EMBOL-X INTRA-AORTIC FILTER: X-SMALL, SMALL, MEDIUM, LARGE, X-LARGE WITH HEPARIN COATED MESH
- K990396 — T-ANASTAFLO
- K991170 — RETROGRADE CARDIOPLEGIA CANNULA WITH DURAFLO TREATMENT, MODEL DII-RC-014
- K983791 — PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA
- K974259 — VENOUS FLEX II PERIPHERAL AND INTRA-OPERATIVE ACCESS VENOUS RETURN CANNULAE
Data sourced from openFDA. This site is unofficial and independent of the FDA.