510(k) K961301 ยท DQD Stethoscope, Electronic
E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120
| Applicant | Delphi Consulting Group, Houston TX, US |
| Decision | Substantially Equivalent, Jun 11, 1996 |
| Received | Apr 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961301
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.