Medical Device Recalls
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1 result found
510(K) Number: K093384 |
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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 Blood Gas Control Level 2 -Model BG5002. In-vitro Diagnostic Quality control of Blood Gas an... | 2 | 03/26/2019 | Randox Laboratories Ltd. |
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