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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K964348
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AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measure... 2 12/22/2018 FEI # 3005529799
Tosoh Bioscience Inc
AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment of calibrators/controls. Par... 3 12/26/2019 FEI # 3005529799
Tosoh Smd Inc
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