510(k) K880898 ยท DXY Implantable Pacemaker Pulse-Generator
MULTICOR AND PACEMAKERS
| Applicant | Tpl-Cordis, Inc., Suffield CT, US |
| Decision | Substantially Equivalent, May 6, 1988 |
| Received | Feb 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880898
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.