510(k) K820657 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR 678 B
| Applicant | Siemens Elema AB, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 15, 1982 |
| Received | Mar 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820657
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.