510(k) K140548 ยท DSI Detector And Alarm, Arrhythmia
CORCAM HEART MONITOR
| Applicant | Corcam Technologia, SA, New York NY, US |
| Decision | Substantially Equivalent, May 23, 2014 |
| Received | Mar 4, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140548
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.