510(k) K151319 ยท DQD Stethoscope, Electronic
Eko Electronic Stethoscope System
| Applicant | Eko Devices, Inc., Berkeley CA, US |
| Decision | Substantially Equivalent, Aug 28, 2015 |
| Received | May 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151319
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.