510(k) K231288 ยท DQA Oximeter
Vyvo
| Applicant | Vyvo Technology Corp.(Vt), Miami FL, US |
| Decision | Substantially Equivalent, Mar 4, 2024 |
| Received | May 4, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231288
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.