510(k) K150314 ยท DQA Oximeter
Masimo MightySat Rx Fingertip Pulse Oximeter
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Oct 22, 2015 |
| Received | Feb 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150314
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.