510(k) K251789 ยท NRY Catheter, Thrombus Retriever
EMBOTRAP III Revascularization Device
| Applicant | Neuravi Limited, Galway, IE |
| Decision | Substantially Equivalent, Sep 25, 2025 |
| Received | Jun 11, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251789
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.