510(k) K133983 ยท MUD Oximeter, Tissue Saturation
INTRA. OX HANDHELD TISSUE OXIMETER
| Applicant | Vioptix, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 12, 2014 |
| Received | Dec 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133983
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.