510(k) K170874 ยท DQD Stethoscope, Electronic
Eko Model E5 System (EME5), Eko DUO
| Applicant | Eko Devices, Inc., Berkeley CA, US |
| Decision | Substantially Equivalent, May 19, 2017 |
| Received | Mar 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170874
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.