510(k) K163459 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Nihon Kohden Vital Sign Telemeter
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Apr 4, 2017 |
| Received | Dec 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163459
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.