Kamiya Biomedical Company, LLC
3 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013 recall (Z-0271-2023) | Kamiya Biomedical Company, LLC | 2022-11-21 |
| K-ASSAY Alpha-1 Microglobulin Reagent Kit. Kit contains: 1 vial Reagent 1, Buffer 50 mL, a recall (Z-0923-2011) | Kamiya Biomedical Company, LLC | 2011-01-19 |
| "K-ASSAY CRP (3) Calibrator E". This product is an IVD calibrator for use on automated cli recall (Z-0973-2010) | Kamiya Biomedical Company, LLC | 2010-03-04 |
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Every clearance here is in the API, with alerts when new ones post.