510(k) K151835 ยท DSI Detector And Alarm, Arrhythmia
Vital Signs Patch System
| Applicant | Lifewatch Technologies , Ltd., Rehovot, IL |
| Decision | Substantially Equivalent, Feb 5, 2016 |
| Received | Jul 6, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151835
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.