510(k) K912391 ยท LQN Latex Agglutination Assay, Rubella
RUBALEX, MODIFICATION
| Applicant | Orion Corp., 20101 Turku, FI |
| Decision | Substantially Equivalent, May 4, 1992 |
| Received | May 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912391
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.