510(k) K963678 ยท DQD Stethoscope, Electronic
CARETONE II
| Applicant | American Telecare, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Feb 24, 1997 |
| Received | Sep 13, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963678
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.