510(k) K233609 ยท DQD Stethoscope, Electronic
CORE 500 Digital Stethoscope
| Applicant | Eko Health, Inc., Emeryville CA, US |
| Decision | Substantially Equivalent, Mar 28, 2024 |
| Received | Nov 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233609
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.