510(k) K990035 ยท DHR System, Test, Rheumatoid Factor
RF
| Applicant | Abbott Laboratories, Irving TX, US |
| Decision | Substantially Equivalent, Mar 8, 1999 |
| Received | Jan 6, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990035
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.