Medical Device Recalls
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1 result found
510(K) Number: K973040 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SPIFE ImmunoFix-6 Kit, Cat. No. 3401, 3401T, For In-Vitro Diagnostic Use. The firm name on the labe... | 2 | 10/04/2019 |
FEI # 1618982 Helena Laboratories, Corp. |
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