Medical Device Recalls
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1 result found
510(K) Number: K040822 |
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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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| Liquichek" ToRCH Plus IgM Control - Positive Liquichek ToRCH Plus IgM Control is intended for use... | 3 | 05/16/2013 |
FEI # 2016706 Bio-rad Laboratories, Inc. |
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