510(k) K073166 ยท KRA Catheter, Continuous Flush
ENDOWAVE INFUSION SYSTEM
| Applicant | Ekos Corp., Bothell WA, US |
| Decision | Unknown, Apr 22, 2008 |
| Received | Nov 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073166
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.