510(k) K233488 · MUD Oximeter, Tissue Saturation
Intra.Ox 2.0 Handheld Tissue Oximeter
| Applicant | Vioptix, Inc., Newark CA, US |
| Decision | Substantially Equivalent, Feb 28, 2024 |
| Received | Oct 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233488
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.