510(k) K823741 ยท LFT Fluorescent Immunoassay, Primidone
ADVANCE EMIT-AED PRIMEDONE ASSAY
| Applicant | Syva Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 7, 1983 |
| Received | Dec 13, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823741
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.