510(k) K134014 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
TEMPUS PRO ACCESSORIES (ULTRASOUND & VIDEO LARYNGOSCOPE PROBE)
| Applicant | Remote Diagnostic Technologies , Ltd., Hampshire, GB |
| Decision | Substantially Equivalent, Aug 12, 2014 |
| Received | Dec 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K134014
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.