510(k) K801106 ยท DXY Implantable Pacemaker Pulse-Generator
MULTICOR (GAMMA) MODEL 336 & MODEL 337
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 8, 1980 |
| Received | May 9, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801106
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.