510(k) K261694 ยท DQD Stethoscope, Electronic
CORE 300 Digital Stethoscope
| Applicant | Eko Health, Inc., Emeryville CA, US |
| Decision | Substantially Equivalent, Jul 23, 2026 |
| Received | May 22, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261694
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.