510(k) K152124 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Tempus IC2
| Applicant | Remote Diagnostics Technologies, Ltd., Basingstoke, GB |
| Decision | Substantially Equivalent, Oct 28, 2015 |
| Received | Jul 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152124
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.