510(k) K863417 ยท DXY Implantable Pacemaker Pulse-Generator
CORDIS MULTICOR II MODEL 402D PACER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Oct 8, 1986 |
| Received | Sep 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863417
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.