Medical Device Recalls
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1 result found
510(K) Number: K092236 |
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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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AdvanDx E. coli/P. aeruginosa PNA FISH Culture Identification Kit for the diagnosis of E. coli and/o... | 2 | 11/29/2010 | AdvanDx, Inc. |
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