510(k) K780453 ยท DXY Implantable Pacemaker Pulse-Generator
STANICOR THETA MODEL 221 CARDIAC PACER
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 30, 1978 |
| Received | Mar 20, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780453
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.