510(k) K060010 ยท DQO Catheter, Intravascular, Diagnostic
NAUTIFLUX
| Applicant | Sedat, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 4, 2006 |
| Received | Jan 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060010
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.