510(k) K842705 ยท DQD Stethoscope, Electronic
MX2 ELECTRONIC STETHOSCOPE
| Applicant | Medmax, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jan 23, 1985 |
| Received | Jul 11, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842705
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.