Medical Device Recalls
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1 result found
510(K) Number: K092704 |
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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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Abbott RealTime CT/NG Assay, List 8L07, in vitro diagnostic; Abbott Molecular Inc., Des Plaines, IL ... | 3 | 02/23/2011 | Abbott Molecular |
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