510(k) K800696 ยท KRE Analyzer, Pacemaker Generator Function, Indirect
ELECTRONIC PACEMAKER WAVEFORM ANALYZER
| Applicant | Instromedix, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 14, 1980 |
| Received | Mar 28, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800696
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.