510(k) K042657 ยท MUD Oximeter, Tissue Saturation
VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
| Applicant | Vioptix, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 10, 2005 |
| Received | Sep 28, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042657
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.