510(k) K830590 ยท KHG Whole Blood Hemoglobin Determination
CORNING 2500 CO-OXIMETER
| Applicant | Corning Medical & Scientific, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 5, 1983 |
| Received | Feb 24, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830590
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.