510(k) K181831 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
IntelliVue Multi-Measurement Module MMX
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Böblingen, DE |
| Decision | Substantially Equivalent, Nov 15, 2018 |
| Received | Jul 9, 2018 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K181831
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.