Medical Device Recalls
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1 result found
510(K) Number: K013373 |
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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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PO2 electrode for Roche AVL OMNI Analyzers. Catalog number BP1734. | 3 | 01/23/2003 | Roche Diagnostics Corp. |
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