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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K102673
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EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro... 2 07/01/2019 FEI # 3002807876
Phadia Ab
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