Medical Device Recalls
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1 result found
510(K) Number: K980120 |
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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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Hc2 System Software Suite 4.0 version 3.0, available as component in Qiagen user guide, catalog #505... | 2 | 06/26/2015 | QIAGEN Gaithersburg, Inc. |
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