510(k) K121232 ยท DBF Ferritin, Antigen, Antiserum, Control
K-ASSAY (R) FERRITIN REAGENT, K-ASSAY (R) FERRITIN CALIBRATOR
| Applicant | Kamiya Biomedical Company, Tukwila WA, US |
| Decision | Substantially Equivalent, May 24, 2012 |
| Received | Apr 24, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121232
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.