510(k) K790666 ยท DXY Implantable Pacemaker Pulse-Generator
VITALITH S 3000 SERIES
| Applicant | Vitatron Medical BV, Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 1, 1979 |
| Received | Apr 6, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790666
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.