510(k) K771924 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
HEARTBEATER
| Applicant | Dunn Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 28, 1977 |
| Received | Oct 13, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771924
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.