Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030873 |
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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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AM1054 Randox Ammonia (NH3), Enzymatic UV Method For the quantitative in vitro determination of A... | 2 | 09/14/2020 | RANDOX LABORATORIES, LTD. |
AM1015 Randox Ammonia (NH3), Enzymatic UV Method For the quantitative in vitro determination of A... | 2 | 09/14/2020 | RANDOX LABORATORIES, LTD. |
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