510(k) K121040 ยท CEM Electrode, Ion Specific, Potassium
SMARTLYTE ELECTROLYTE ANALYZER
| Applicant | Diamond Diagnostics, Inc., Holliston MA, US |
| Decision | Substantially Equivalent, Aug 30, 2012 |
| Received | Apr 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121040
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.