510(k) K230111 ยท DQD Stethoscope, Electronic
CORE 500 Digital Stethoscope
| Applicant | Eko Devices, Inc., Oakland CA, US |
| Decision | Substantially Equivalent, May 26, 2023 |
| Received | Jan 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230111
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.