510(k) K910539 ยท DHR System, Test, Rheumatoid Factor
RHEUMAJET RF
| Applicant | Biokit USA, Inc., Barcelona, ES |
| Decision | Substantially Equivalent, Apr 5, 1991 |
| Received | Jan 28, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910539
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.