510(k) K850651 ยท DXY Implantable Pacemaker Pulse-Generator
PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Apr 1, 1985 |
| Received | Feb 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850651
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.