Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K970684 |
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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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Lactate Dehydrognease P-L, (UV), Catalog Number LD3818 - Product Usage: device intended for the quan... | 2 | 09/12/2020 | Randox Laboratories Ltd. |
Lactate Dehydrogenase L-P, (LDH) (NAO), Catalog Number LD3842 - Product Usage: device intended for t... | 2 | 09/12/2020 | Randox Laboratories Ltd. |
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