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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K970684
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Lactate Dehydrognease P-L, (UV), Catalog Number LD3818 - Product Usage: device intended for the quan... 2 09/12/2020 FEI # 1000361607
Randox Laboratories Ltd.
Lactate Dehydrogenase L-P, (LDH) (NAO), Catalog Number LD3842 - Product Usage: device intended for t... 2 09/12/2020 FEI # 1000361607
Randox Laboratories Ltd.
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