510(k) K801324 ยท DXY Implantable Pacemaker Pulse-Generator
SIEMENS-ELEMA PULSE GENERATOR 668
| Applicant | Siemens Elema AB, Walker MI, US |
| Decision | Substantially Equivalent, Dec 1, 1980 |
| Received | Jun 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801324
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.