510(k) K840863 ยท DHR System, Test, Rheumatoid Factor
SERATEST RF LATEX DETERMINATION
| Applicant | Seragen Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 4, 1984 |
| Received | Feb 24, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840863
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.