510(k) K900300 ยท CEM Electrode, Ion Specific, Potassium
LYTENING 2Z LYTENING SYSTEM 31
| Applicant | Baxter Healthcare Corp, Santa Ana CA, US |
| Decision | Substantially Equivalent, Mar 1, 1990 |
| Received | Jan 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900300
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.