510(k) K833519 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR MODEL 688
| Applicant | Burditt & Calkins-Siemens-Elema, Walker MI, US |
| Decision | Substantially Equivalent, Jan 30, 1984 |
| Received | Oct 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833519
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.