510(k) K790432 ยท DXY Implantable Pacemaker Pulse-Generator
MICROLITH MODELS 505;605;507;607;703;803
| Applicant | Cardiac Pacemakers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 20, 1979 |
| Received | Mar 2, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790432
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.