510(k) K213794 ยท DQD Stethoscope, Electronic
Eko Murmur Analysis Software (EMAS)
| Applicant | Eko Devices, Inc., Oakland CA, US |
| Decision | Substantially Equivalent, Jun 29, 2022 |
| Received | Dec 6, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213794
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.