510(k) K173768 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Tempus Pro Patient Monitor
| Applicant | Remote Diagnostic Technologies , Ltd., Basingstoke, GB |
| Decision | Substantially Equivalent, Jan 10, 2018 |
| Received | Dec 11, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173768
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.