510(k) K250751 ยท DQO Catheter, Intravascular, Diagnostic
DualView Catheter
| Applicant | Terumo Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Jul 17, 2025 |
| Received | Mar 12, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250751
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.