510(k) K896433 ยท LQN Latex Agglutination Assay, Rubella
MODIFIED RUBAGEN
| Applicant | Biokit USA, Inc., Barcelona, ES |
| Decision | Substantially Equivalent, Nov 29, 1989 |
| Received | Nov 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896433
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.