510(k) K812882 ยท DHR System, Test, Rheumatoid Factor
RHEUMATEX
| Applicant | Armkel, LLC, Walker MI, US |
| Decision | Substantially Equivalent, Oct 26, 1981 |
| Received | Oct 14, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812882
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.