510(k) K823878 ยท DXY Implantable Pacemaker Pulse-Generator
IMPLANTABLE PACEMAKER PULSE GEN, MODELS 241 & 242
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Mar 24, 1983 |
| Received | Dec 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823878
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.