510(k) K220383 ยท KRD Device, Vascular, For Promoting Embolization
LOBO Vascular Occlusion System (models LOBO-7 and LOBO-9)
| Applicant | Okami Medical, Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Apr 29, 2022 |
| Received | Feb 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220383
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.