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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: K931059
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IMx Rubella IgM Reagent Kit, 100 tests, list 7A24-20; Abbott Laboratories, Abbott Park, IL 60064 3 08/13/2003 FEI # 1415939
Abbott Laboratories HPD/ADD/GPRD
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