510(k) K791095 ยท DXY Implantable Pacemaker Pulse-Generator
LITHICRON MODEL 0401, PACEMAKER
| Applicant | Medcor, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 10, 1979 |
| Received | Jun 12, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791095
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.