510(k) K843896 ยท DHR System, Test, Rheumatoid Factor
RHEUMADX LATEX AGGLUTINATION RHEUMATOID
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Oct 25, 1984 |
| Received | Oct 3, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843896
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.