510(k) K913467 ยท LLA Direct Agglutination Test, Toxoplasma Gondii
TOXOGEN
| Applicant | Biokit USA, Inc., Barcelona, ES |
| Decision | Substantially Equivalent, Jan 11, 1993 |
| Received | Aug 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913467
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.