510(k) K151269 ยท DSI Detector And Alarm, Arrhythmia
ECG Mini System Continuous ECG Monitor and Arrhythmia Detector
| Applicant | Lifewatch Technologies , Ltd., Rehovot, IL |
| Decision | Substantially Equivalent, Jan 15, 2016 |
| Received | May 13, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151269
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.