510(k) K831860 ยท DXY Implantable Pacemaker Pulse-Generator
GENERATOR, PULSE, PACEMAKER #532
| Applicant | Vitatron Medical BV, Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 27, 1983 |
| Received | Jun 10, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831860
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.