510(k) K813101 ยท DXY Implantable Pacemaker Pulse-Generator
CARDIOBEEPER MEMORY MONITOR
| Applicant | Survival Technology, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 27, 1981 |
| Received | Nov 3, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813101
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.