510(k) K181623 ยท MUD Oximeter, Tissue Saturation
Clarifi Imaging System
| Applicant | Modulated Imaging, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jul 19, 2018 |
| Received | Jun 20, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181623
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.