510(k) K841233 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR 678L
| Applicant | Siemens Elema AB, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 6, 1984 |
| Received | Mar 22, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841233
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.