510(k) K223574 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
IntelliVue Patient Monitor MX400 (866060), IntelliVue Patient Monitor MX450 (866062), IntelliVue Patient Monitor MX500 (866064), IntelliVue Patient Monitor MX550 (866066)
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Böblingen, DE |
| Decision | Substantially Equivalent, Aug 22, 2023 |
| Received | Nov 30, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223574
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.