510(k) K880432 ยท DXY Implantable Pacemaker Pulse-Generator
VICOR PACER, MODEL 410A
| Applicant | Tpl-Cordis, Inc., Suffield CT, US |
| Decision | Substantially Equivalent, Feb 22, 1988 |
| Received | Jan 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880432
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.