510(k) K840748 ยท DXY Implantable Pacemaker Pulse-Generator
LITHIUM PACEMAKER 811-811L & 811XL
| Applicant | Omikron Scientific, Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Aug 3, 1984 |
| Received | Feb 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840748
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.