510(k) K160656 ยท DXR Ballistocardiograph
CorSens
| Applicant | Corsens Medical , Ltd., Tel Aviv, IL |
| Decision | Substantially Equivalent, Nov 21, 2016 |
| Received | Mar 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160656
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.