510(k) K152305 ยท DSI Detector And Alarm, Arrhythmia
Nihon Kohden Afib Detection Program QP-039P
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Apr 8, 2016 |
| Received | Aug 14, 2015 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K152305
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.