510(k) K884733 ยท DXY Implantable Pacemaker Pulse-Generator
AFP MODEL 262T PULSE GENERATOR
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Feb 10, 1989 |
| Received | Nov 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884733
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.