510(k) K142180 ยท DSI Detector And Alarm, Arrhythmia
TELESENSE
| Applicant | Scottcare Corporation, Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 12, 2014 |
| Received | Aug 8, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142180
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.