510(k) K131044 ยท DQD Stethoscope, Electronic
SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION
| Applicant | Diacoustic Medical Devices (Pty) , Ltd., Crofton MD, US |
| Decision | Substantially Equivalent, Sep 4, 2013 |
| Received | Apr 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131044
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.