510(k) K202483 ยท DQD Stethoscope, Electronic
MyHomeDoc
| Applicant | Myhomedoc , Ltd., Ra'Anana, IL |
| Decision | Substantially Equivalent, Mar 23, 2021 |
| Received | Aug 28, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202483
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.