510(k) K213200 ยท KRD Device, Vascular, For Promoting Embolization
Solus Gold Embolization Device
| Applicant | Artio Medical, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Mar 21, 2022 |
| Received | Sep 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213200
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.