510(k) K851418 ยท DXY Implantable Pacemaker Pulse-Generator
OMNI-ATRICOR MODEL 308A
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jun 11, 1985 |
| Received | Apr 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851418
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.