510(k) K822229 ยท LFT Fluorescent Immunoassay, Primidone
PRIMIDONE FLUORESCENT IMMUNOASSAY
| Applicant | American Diagnostic Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 12, 1982 |
| Received | Jul 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822229
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.