510(k) K855081 ยท DXY Implantable Pacemaker Pulse-Generator
PHOENIX MODELS 250/251 PULSE GENERATORS
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Mar 7, 1986 |
| Received | Dec 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855081
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.