Medical Device Recalls
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1 result found
510(K) Number: K110846 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for in ... | 3 | 09/23/2019 | Randox Laboratories Ltd. |
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