Ekos Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ekos Corp. - FDA 510(k) Cleared Devices
23
Total
18
Cleared
0
Denied
Ekos Corp. has 18 FDA 510(k) cleared cardiovascular devices. Based in Bothell, US.
Historical record: 18 cleared submissions from 2003 to 2008.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ekos Corp.
23 devices
Cleared
Jun 26, 2008
EKOSONIC ENDOVASCULAR SYSTEM WITH RAPID PULSE MODULATION
Cardiovascular
30d
Cleared
Apr 30, 2008
EndoWave Infusion System
Cardiovascular
77d
Cleared
Apr 22, 2008
ENDOWAVE INFUSION SYSTEM
Cardiovascular
165d
Cleared
Oct 04, 2007
ENDOWAVE INFUSION SYSTEM
Cardiovascular
28d
Cleared
Aug 10, 2007
ENDOWAVE INFUSION SYSTEM
Cardiovascular
28d
Cleared
Aug 06, 2007
EKOS MICRO-INFUSION SYSTEM
Cardiovascular
244d
Cleared
Dec 05, 2006
NEUROWAVE MICRO-INFUSION SYSTEM
Neurology
99d
Cleared
Nov 22, 2006
MICRO-INFUSION SYSTEM
Cardiovascular
86d
Cleared
Mar 09, 2006
LYSUS INFUSION SYSTEM
Cardiovascular
20d
Cleared
Feb 07, 2006
LYSUS INFUSION SYSTEM
Cardiovascular
27d
Cleared
Jan 06, 2006
EKOS MICRO-INFUSION SYSTEM
Neurology
28d
Cleared
Dec 30, 2005
EKOS MICRO-INFUSION SYSTEM
Cardiovascular
21d