510(k) K212908 ยท NRY Catheter, Thrombus Retriever
EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device
| Applicant | Neuravi, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Oct 13, 2021 |
| Received | Sep 13, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212908
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.