510(k) K901039 ยท CEM Electrode, Ion Specific, Potassium
IONOMETER EH
| Applicant | Fresenius USA, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Jun 28, 1990 |
| Received | Mar 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901039
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.