510(k) K791751 ยท DXY Implantable Pacemaker Pulse-Generator
EDWARDS PACEMAKER 30 UNIPOLAR GENERATOR
| Applicant | Edwards Pacemaker Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 26, 1979 |
| Received | Sep 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791751
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.