Medical Device Recalls
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1 result found
510(K) Number: K953115 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AxSYM Drugs of Abuse/Toxicology Assay Disk Version 8.0; List Number: 3D54-08; Abbott La boratories, ... | 3 | 05/14/2008 |
FEI # 1415939 Abbott Laboratories |
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