510(k) K822639 ยท DXY Implantable Pacemaker Pulse-Generator
AFP SYSTEM PULSE GENERATOR MODEL 261/262
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 18, 1983 |
| Received | Sep 1, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822639
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.