Medical Device Recalls
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1 result found
510(K) Number: K990023 |
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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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Hybrid Capture II CT-ID Test, Catalog #5135-1050IVT, (labeled for export only). | 2 | 03/19/2003 | Digene Corp |
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