510(k) K844360 ยท DXY Implantable Pacemaker Pulse-Generator
CORDIS MULTICOR S 330A & 331A CARDIAC PACEMAKERS
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jun 18, 1985 |
| Received | Nov 13, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844360
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.