510(k) K220567 ยท KRD Device, Vascular, For Promoting Embolization
Easi-Vue embolic microspheres System
| Applicant | Abk Biomedical, Inc., Halifax, CA |
| Decision | Substantially Equivalent, Sep 7, 2022 |
| Received | Feb 28, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220567
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.