510(k) K833619 ยท KRC Tester, Electrode, Surface, Electrocardiographic
CONDUCTANCE METER
| Applicant | Circadian, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 27, 1984 |
| Received | Oct 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833619
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.