510(k) K782023 ยท DXY Implantable Pacemaker Pulse-Generator
MICROLITH A MODEL 803
| Applicant | Cardiac Pacemakers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 22, 1978 |
| Received | Dec 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782023
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.