510(k) K851968 ยท DXY Implantable Pacemaker Pulse-Generator
CORDIS MULTICOR ST, MODEL 350A
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 14, 1986 |
| Received | May 7, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851968
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.