510(k) K842315 ยท CEM Electrode, Ion Specific, Potassium
ULTRA LYTE ANALYZER I 100
| Applicant | Ultra Quest Diagnostics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Aug 2, 1984 |
| Received | Jun 12, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842315
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.