Medical Device Recalls
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1 result found
510(K) Number: K182042 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Randox CALCIUM (Ca) COLORIMETRIC METHOD RX DAYTONA PLUS Cat. No. CA 8309 R1, Arsenazo Reagent 4 x ... | 2 | 02/15/2019 |
FEI # 1000361607 Randox Laboratories Ltd. |
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