510(k) K800054 ยท CEM Electrode, Ion Specific, Potassium
KODAK EKTACHEM ELECTROLYTE ANALYZER
| Applicant | Eastman Kodak Company, Walker MI, US |
| Decision | Substantially Equivalent, Feb 5, 1980 |
| Received | Jan 9, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800054
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.