510(k) K223670 ยท DPS Electrocardiograph
MESI mTablet ECG Diagnostic System, MESI mTablet ECG
| Applicant | Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O., Ljubljana, SI |
| Decision | Substantially Equivalent, Jul 28, 2023 |
| Received | Dec 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223670
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.