510(k) K830344 ยท DXY Implantable Pacemaker Pulse-Generator
SIEMENS-ELMA PULSE GENERATOR #718
| Applicant | Burditt & Calkins-Siemens-Elema, Mchenry IL, US |
| Decision | Substantially Equivalent, May 27, 1983 |
| Received | Feb 2, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830344
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.