Medical Device Recalls
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1 result found
510(K) Number: K964349 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement ... | 2 | 12/22/2018 | Tosoh Bioscience Inc |
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