Medical Device Recalls
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1 result found
510(K) Number: K013785 |
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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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ProbeChek Vysis UroVysion Control Slides, for Fluorescence in situ Hybridization (FISH) using Vysis ... | 3 | 07/20/2004 | Vysis |
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