510(k) K231671 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
IntelliVue Patient Monitor MX750 (866471), IntelliVue Patient Monitor MX850 (866470), IntelliVue 4-Slot Module Rack FMX-4 (866468)
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Böblingen, DE |
| Decision | Substantially Equivalent, Dec 19, 2023 |
| Received | Jun 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231671
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.