510(k) K211338 ยท NRY Catheter, Thrombus Retriever
EMBOTRAP III Revascularization Device
| Applicant | Neuravi, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Jul 30, 2021 |
| Received | May 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211338
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.