510(k) K142394 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Masimo Root Monitoring System and Accesories
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 25, 2014 |
| Received | Aug 27, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142394
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.