510(k) K897110 ยท CEM Electrode, Ion Specific, Potassium
SATELLITE K+ BLOOD POTASSIUM MONITORING SYSTEM
| Applicant | Medisense, Inc., Cambridge MA, US |
| Decision | Substantially Equivalent, Feb 27, 1990 |
| Received | Dec 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897110
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.