Ekos Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ekos Corporation - FDA 510(k) Cleared Devices
Recent clearances: EKOS PE Endovascular Device with Control System 4.0 (CS4.0)
2
Total
2
Cleared
0
Denied
Ekos Corporation has 2 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 2 cleared submissions from 2011 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ekos Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ekos Corporation
2 devices