510(k) K890048 ยท LLA Direct Agglutination Test, Toxoplasma Gondii
QUIK-DOT TOXOPLASMOSIS
| Applicant | Ampcor, Inc., Bridgeport NJ, US |
| Decision | Substantially Equivalent, Jun 9, 1989 |
| Received | Jan 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890048
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.