FDA 510(k) Applications Submitted by KAMIYA BIOMEDICAL COMPANY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121232 | 04/24/2012 | K-ASSAY (R) FERRITIN REAGENT, K-ASSAY (R) FERRITIN CALIBRATOR | KAMIYA BIOMEDICAL COMPANY |
| K192727 | 09/27/2019 | K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2) | Kamiya Biomedical Company |
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