Ekos Ultrasound Infusion System
FDA 510(k) K041826 · Ekos Corp.
510(k) numberK041826
Submission
- Device name
- Ekos Ultrasound Infusion System
- Applicant
- Ekos Corp.
Bothell, WA, US - Received
- July 7, 2004
- Decision date
- April 27, 2005
- Decision
- Unknown (SESU)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- NUI – Ultrasound, Infusion, System
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1200
- Specialty
- Cardiovascular
For regional infusion of contrast materials into selected vessels in the neuro-vasculature. The device may be used for controlled, regional infusion into selected vessels and is not intended for use in the coronary vasculature.
Other 510(k)s with product code NUI
More from Ekos Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K200648 | EKOS PE Endovascular Device with Control System 4.0 (CS4.0)QEY · Special | 08/17/2020SE |
| K111705 | Ekosonic Endovascular SystemQEY · Traditional | 08/03/2011SE |
| K081467 | Ekosonic Endovascular System with Rapid Pulse ModulationQEY · Special | 06/26/2008SE |
| K080392 | EndoWave Infusion SystemQEY · Special | 04/30/2008SE |
| K073166 | Endowave Infusion SystemKRA · Traditional | 04/22/2008SESU |
| K072507 | Endowave Infusion SystemQEY · Special | 10/04/2007SE |
| K071933 | Endowave Infusion SystemQEY · Special | 08/10/2007SE |
| K063620 | Ekos Micro-Infusion SystemQEY · Traditional | 08/06/2007SESU |
| K062508 | Neurowave Micro-Infusion SystemNUI · Special | 12/05/2006SESU |
| K062507 | Micro-Infusion SystemQEY · Special | 11/22/2006SE |
Questions and answers
When was Ekos Ultrasound Infusion System cleared by the FDA?
Ekos Ultrasound Infusion System (K041826) received a 510(k) decision of Unknown on April 27, 2005, 294 days after the submission was received.
What is the product code of K041826?
The FDA product code is NUI – Ultrasound, Infusion, System, a Class II (moderate risk) device regulated under 21 CFR 870.1200.