Medical Device Manufacturer · US , Bothell , WA

Ekos Corp. - FDA 510(k) Cleared Devices

23 submissions · 18 cleared · Since 2003
23
Total
18
Cleared
0
Denied

FDA 510(k) Regulatory Record - Ekos Corp. Neurology ✕

4 devices
1-4 of 4
Cleared Dec 05, 2006
NEUROWAVE MICRO-INFUSION SYSTEM
K062508 · NUI
Neurology · 99d
Cleared Jan 06, 2006
EKOS MICRO-INFUSION SYSTEM
K053437 · NUI
Neurology · 28d
Cleared Jun 10, 2005
EKOS MICRO-INFUSION SYSTEM
K051225 · NUI
Neurology · 29d
Cleared Apr 27, 2005
EKOS ULTRASOUND INFUSION SYSTEM
K041826 · NUI
Neurology · 294d
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