510(k) K191676 ยท MUD Oximeter, Tissue Saturation
Intra.Ox 2.0 Handheld Tissue Oximeter
| Applicant | Vioptix, Inc., Newark CA, US |
| Decision | Substantially Equivalent, Sep 16, 2019 |
| Received | Jun 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191676
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.