510(k) K790690 ยท DXY Implantable Pacemaker Pulse-Generator
OMNI-STANICOR-(THETA) MODEL 217
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 16, 1979 |
| Received | Apr 10, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790690
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.