510(k) K861422 ยท DXY Implantable Pacemaker Pulse-Generator
PACESETTER/SIEMENS PULSE GENERA W/VS-1 HEAD CAVITY
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Jun 26, 1986 |
| Received | Apr 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861422
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.