510(k) K880300 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
CARDIOBEEPER(R) III
| Applicant | Survival Technology, Inc., Bethesda MD, US |
| Decision | Substantially Equivalent, May 12, 1988 |
| Received | Jan 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880300
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.