510(k) K792232 ยท DXY Implantable Pacemaker Pulse-Generator
UNIFOCAL 3-2 MODELS UNIPOLAR & BIPOLAR
| Applicant | American Pacemaker Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 27, 1979 |
| Received | Nov 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792232
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.