510(k) K912030 ยท CBZ Analyzer, Ion, Hydrogen-Ion (Ph), Blood-Phase, Indwelling
CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED
| Applicant | 3M Company, Tustin CA, US |
| Decision | Substantially Equivalent, Oct 30, 1991 |
| Received | May 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912030
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.