510(k) K800838 ยท DXY Implantable Pacemaker Pulse-Generator
ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.
| Applicant | Arco Medical Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 4, 1980 |
| Received | Apr 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800838
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.