510(k) K172226 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MX40 Release B.07
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Nov 9, 2017 |
| Received | Jul 25, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172226
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.