510(k) K780238 ยท DXY Implantable Pacemaker Pulse-Generator
PACEMAKER, PROLITH 23U. PULSE GENERATOR
| Applicant | Edwards Pacemaker Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 15, 1978 |
| Received | Feb 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780238
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.