510(k) K800746 ยท DXY Implantable Pacemaker Pulse-Generator
UNIFOCAL VP, MODELS 7501 AND 7502
| Applicant | American Pacemaker Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 16, 1980 |
| Received | Apr 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800746
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.