510(k) K832959 ยท KRE Analyzer, Pacemaker Generator Function, Indirect
PACEMAKER SYS. ANALYZER 378
| Applicant | Siemens Elema AB, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 14, 1983 |
| Received | Aug 30, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832959
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.