Medical Device Recalls
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1 result found
510(K) Number: K113319 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycli... | 2 | 03/12/2020 |
FEI # 3003572099 Qiagen Sciences LLC |
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