510(k) K791784 ยท DXY Implantable Pacemaker Pulse-Generator
CORDIS BIPOLAR PACER CONNECTOR SYSTEM
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Sep 28, 1979 |
| Received | Sep 12, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791784
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.