510(k) K881904 ยท DXY Implantable Pacemaker Pulse-Generator
CHANGE TO CATHODE POWDER SPECIFICATION
| Applicant | Telectronics and Cordis Pacing Systems, Miami FL, US |
| Decision | Substantially Equivalent, Jul 22, 1988 |
| Received | May 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881904
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.