510(k) K233924 ยท QJP Catheter, Percutaneous, Neurovasculature
EMBOGUARD Balloon Guide Catheter
| Applicant | Neuravi Limited, Galway, IE |
| Decision | Substantially Equivalent, Apr 18, 2024 |
| Received | Dec 13, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233924
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.