510(k) K262798 ยท KRD Device, Vascular, For Promoting Embolization
LOBO Vascular Occlusion System
| Applicant | Okami Medical, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Oct 6, 2026 |
| Received | Aug 7, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262798
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.