Medical Device Recalls
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1 result found
510(K) Number: K931059 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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IMx Rubella IgM Reagent Kit, 100 tests, list 7A24-20; Abbott Laboratories, Abbott Park, IL 60064 | 3 | 08/13/2003 | Abbott Laboratories HPD/ADD/GPRD |
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