510(k) K234123 · KRD Device, Vascular, For Promoting Embolization
Easi-Vue® embolic microspheres System
| Applicant | Abk Biomedical, Inc., Halifax, CA |
| Decision | Substantially Equivalent, Feb 13, 2024 |
| Received | Dec 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234123
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.