510(k) K812610 ยท DXY Implantable Pacemaker Pulse-Generator
SIEMENS-ELEMA PULSE GENERATOR 668 B
| Applicant | Siemens Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 10, 1981 |
| Received | Sep 15, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812610
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.