510(k) K192137 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
IntelliVue Patient Monitor MX500, IntelliVue Patient Monitor MX550
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Böblingen, DE |
| Decision | Substantially Equivalent, Sep 11, 2020 |
| Received | Aug 7, 2019 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K192137
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.