510(k) K181956 ยท DQA Oximeter
Masimo MightySat Rx Fingertip Pulse Oximeter
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Jan 23, 2019 |
| Received | Jul 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181956
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.