510(k) K041826 ยท NUI Ultrasound, Infusion, System
EKOS ULTRASOUND INFUSION SYSTEM
| Applicant | Ekos Corp., Bothell WA, US |
| Decision | Unknown, Apr 27, 2005 |
| Received | Jul 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041826
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.