Randox Laboratories
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| CRP Immunoturbidimetric reagent. Intended for the quantitative in vitro determination of C recall (Z-1286-2023) | Randox Laboratories | 2024-09-30 |
| Liquid Urine Control Level 3 For Professional Use in the quality control monitoring of In- recall (Z-2167-2017) | Randox Laboratories | 2017-05-26 |
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Every clearance here is in the API, with alerts when new ones post.