Edwards Lifesciences Research Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Edwards Lifesciences Research Medical - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Edwards Lifesciences Research Medical has 6 FDA 510(k) cleared medical devices. Based in Midvale, US.
Historical record: 6 cleared submissions from 1998 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Edwards Lifesciences Research Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Edwards Lifesciences Research Medical
6 devices
Cleared
Jan 31, 2008
18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION...
Cardiovascular
43d
Cleared
Sep 27, 2006
MODIFICATION TO EMBOL-X INTRA-AORTIC FILTER: X-SMALL, SMALL, MEDIUM, LARGE,...
Cardiovascular
37d
Cleared
Oct 01, 1999
T-ANASTAFLO
Cardiovascular
234d
Cleared
Jul 02, 1999
RETROGRADE CARDIOPLEGIA CANNULA WITH DURAFLO TREATMENT, MODEL DII-RC-014
Cardiovascular
86d
Cleared
Jun 11, 1999
PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA
Cardiovascular
227d
Cleared
Dec 01, 1998
VENOUS FLEX II PERIPHERAL AND INTRA-OPERATIVE ACCESS VENOUS RETURN CANNULAE
Cardiovascular
383d