510(k) K800026 ยท DXY Implantable Pacemaker Pulse-Generator
MICROTHIN-DI
| Applicant | Cardiac Pacemakers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 31, 1980 |
| Received | Jan 7, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800026
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.