510(k) K800268 ยท DHR System, Test, Rheumatoid Factor
AUTOMATED RHEMATOID FACTOR TEST (ARFT)
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Feb 21, 1980 |
| Received | Feb 6, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800268
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.