510(k) K781042 ยท DXY Implantable Pacemaker Pulse-Generator
PROLITH 23S PACEMAKER
| Applicant | Edwards Pacemaker Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 27, 1978 |
| Received | Jun 20, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781042
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.