510(k) K843741 ยท GMP Antisera, Control For Nontreponemal Tests
RPR TEST REDITEST
| Applicant | Biokit USA, Inc., Barcelona, Spain, US |
| Decision | Substantially Equivalent, Oct 25, 1984 |
| Received | Sep 25, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843741
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.