Medical Device Recalls
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1 result found
510(K) Number: K984074 |
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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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Architect Total T4 MasterCheck; a single (specified) analyte control (assayed and unassayed); list 6... | 3 | 07/31/2008 | Abbott Laboratories |
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