510(k) K884228 ยท CBZ Analyzer, Ion, Hydrogen-Ion (Ph), Blood-Phase, Indwelling
CDI(R) 2000 BLOOD GAS MONITOR
| Applicant | Cardiovascular Devices, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 30, 1989 |
| Received | Oct 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884228
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.