510(k) K790562 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR MODEL 61 AND 128
| Applicant | Ela Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 8, 1979 |
| Received | Mar 19, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790562
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.