510(k) K113105 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
TEMPUSIC PATIENT MONITOR
| Applicant | Remote Diagnostic Technologies , Ltd., Hampshire, GB |
| Decision | Substantially Equivalent, Dec 15, 2011 |
| Received | Oct 20, 2011 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K113105
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.