510(k) K151812 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PATIENT MONITORS VARIOUS MODELS
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Jan 26, 2016 |
| Received | Jul 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151812
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.