510(k) K251702 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
IntelliVue Patient Monitor MX750; IntelliVue Patient Monitor MX850; IntelliVue 4-Slot Module Rack FMX-4 (866471 866470 866468 )
| Applicant | Philips Medizin Systeme Böblingen GmbH, Böblingen, DE |
| Decision | Substantially Equivalent, Nov 10, 2025 |
| Received | Jun 2, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251702
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.