510(k) K173452 ยท NRY Catheter, Thrombus Retriever
EmboTrap ll Revascularization Device
| Applicant | Neuravi, Ltd., Galway, IE |
| Decision | Substantially Equivalent, May 9, 2018 |
| Received | Nov 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173452
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.