510(k) K993623 ยท DQD Stethoscope, Electronic
GEMINI E
| Applicant | Allen Medical Instruments Corp., Newport Beach CA, US |
| Decision | Substantially Equivalent, Jun 23, 2000 |
| Received | Oct 26, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993623
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.