510(k) K231276 ยท DSI Detector And Alarm, Arrhythmia
SmartCardia 7L Platform
| Applicant | Smartcardia SA, Lausanne, CH |
| Decision | Substantially Equivalent, Aug 30, 2023 |
| Received | May 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231276
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.