510(k) K851861 ยท DXY Implantable Pacemaker Pulse-Generator
PROGRAMALITH III MODEL 249 PULSE GENERATOR
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, May 16, 1985 |
| Received | Apr 26, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851861
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.