FDA 510(k) Applications for Medical Device Product Code "NUI"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K051225 | EKOS CORP. | EKOS MICRO-INFUSION SYSTEM | 06/10/2005 |
K053437 | EKOS CORP. | EKOS MICRO-INFUSION SYSTEM | 01/06/2006 |
K041826 | EKOS CORP. | EKOS ULTRASOUND INFUSION SYSTEM | 04/27/2005 |
K062508 | EKOS CORP. | NEUROWAVE MICRO-INFUSION SYSTEM | 12/05/2006 |