510(k) K170567 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Tempus Pro Patient Monitor
| Applicant | Remote Diagnostic Technologies , Ltd., Basingstoke, GB |
| Decision | Substantially Equivalent, Jul 6, 2017 |
| Received | Feb 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170567
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.