Medical Device Recalls
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1 result found
510(K) Number: K934544 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Free T4 Control Pack, list 9C03-10; the kit consists of 3 bottles of controls, L - 0.7, M - 1.2 and ... | 3 | 08/13/2003 |
FEI # 1415939 Abbott Laboratories HPD/ADD |
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