510(k) K854790 ยท DXY Implantable Pacemaker Pulse-Generator
CERYX PACEMAKER MODELS 114, 314 & 614
| Applicant | Vitatron Medical BV, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 28, 1986 |
| Received | Nov 29, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854790
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.