510(k) K163584 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
M3290B Philips IntelliVue Information Center iX
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Jul 7, 2017 |
| Received | Dec 20, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163584
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.