510(k) K240900 · DXF Catheter, Septostomy
HOTWIRE RF Guidewire
| Applicant | Atraverse Medical, Cardiff By The Sea CA, US |
| Decision | Substantially Equivalent, May 1, 2024 |
| Received | Apr 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240900
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.