510(k) K900818 ยท LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii
VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM (VIDAS) TOXO.
| Applicant | Vitek Systems, Inc., Hazelwood MI, US |
| Decision | Substantially Equivalent, Apr 30, 1990 |
| Received | Feb 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900818
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.