510(k) K885267 ยท DXY Implantable Pacemaker Pulse-Generator
VS-1 MODEL NUMBER 251K PULSE GENERATOR
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Mar 28, 1989 |
| Received | Dec 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885267
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.