510(k) K820356 ยท DXY Implantable Pacemaker Pulse-Generator
MULTICOR (GAMMA) 402 CARDIAC PACER
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 18, 1982 |
| Received | Feb 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820356
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.