510(k) K180017 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MX40 Release C.01
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Jul 24, 2018 |
| Received | Jan 2, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180017
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.