510(k) K881711 ยท DXY Implantable Pacemaker Pulse-Generator
VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA.
| Applicant | Telectronics and Cordis Pacing Systems, Miami FL, US |
| Decision | Substantially Equivalent, May 26, 1988 |
| Received | Apr 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881711
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.