510(k) K212057 ยท KRD Device, Vascular, For Promoting Embolization
Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS
| Applicant | Artventive Medical Group, Inc., San Marcos CA, US |
| Decision | Substantially Equivalent, Mar 1, 2022 |
| Received | Jul 1, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212057
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.