510(k) K801183 ยท LDE Stethoscope, Manual
CONPHAR DUAL HEAD STETHOSCOPE
| Applicant | Conphar, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 4, 1980 |
| Received | May 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801183
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.