510(k) K811691 ยท DXY Implantable Pacemaker Pulse-Generator
CORDIS OMNI-ARTICOR CARDIAC PACER #308
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 20, 1981 |
| Received | Jun 15, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811691
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.