510(k) K790014 ยท DXY Implantable Pacemaker Pulse-Generator
BIPOLAR, STANICOR LAMBDA MODEL 236,235
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 8, 1979 |
| Received | Jan 3, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790014
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.