Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K923504 |
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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 Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma.... | 2 | 07/20/2022 | Randox Laboratories Ltd. |
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF... | 2 | 12/01/2021 | Randox Laboratories Ltd. |
Advia Chemistry Assay: LDL Cholesterol, Direct | 2 | 05/11/2016 | Siemens Healthcare Diagnostics, Inc. |
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