510(k) K153477 ยท DSI Detector And Alarm, Arrhythmia
EMMa Electronic Monitoring Management
| Applicant | Vitasystems GmbH, Mannheim, DE |
| Decision | Substantially Equivalent, May 25, 2016 |
| Received | Dec 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153477
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.