510(k) K760043 ยท DHR System, Test, Rheumatoid Factor
TEST, RHEUM. ARTH., CARD (MACRO-VUE)
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Aug 3, 1976 |
| Received | Jun 15, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760043
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.