510(k) K792216 ยท DXY Implantable Pacemaker Pulse-Generator
ARCOLITH 2100-CARDIAC PULSE GENERATOR
| Applicant | Arco Medical Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 29, 1979 |
| Received | Nov 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792216
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.