510(k) K182532 ยท DSI Detector And Alarm, Arrhythmia
Liba3 System
| Applicant | National Cardiac, Inc., Escondido CA, US |
| Decision | Substantially Equivalent, May 15, 2019 |
| Received | Sep 14, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182532
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.