510(k) K242130 ยท POK Computer-Assisted Diagnostic Software For Lesions Suspicious For Cancer
Koios DS
| Applicant | Koios Medical, Inc., New York NY, US |
| Decision | Substantially Equivalent, Nov 15, 2024 |
| Received | Jul 22, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242130
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.