510(k) K200776 ยท DQD Stethoscope, Electronic
Eko CORE
| Applicant | Eko Devices, Inc., Oakland CA, US |
| Decision | Substantially Equivalent, Apr 6, 2020 |
| Received | Mar 25, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200776
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.