510(k) K790873 ยท DXY Implantable Pacemaker Pulse-Generator
MODEL 221 PROGRAMALITH PULSE GENERATOR
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 20, 1979 |
| Received | May 7, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790873
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.