510(k) K801022 ยท KRE Analyzer, Pacemaker Generator Function, Indirect
ULTRA-CHEK PACEMAKER MONITOR
| Applicant | Powers Medical Systmes, Walker MI, US |
| Decision | Substantially Equivalent, Jun 17, 1980 |
| Received | Apr 30, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801022
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.