510(k) K841225 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR 689, 689B & 689L
| Applicant | Siemens Elema AB, Chicago IL, US |
| Decision | Substantially Equivalent, Dec 3, 1984 |
| Received | Mar 22, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841225
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.