Medical Device Recalls
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1 result found
510(K) Number: K981812 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for... | 2 | 05/16/2016 | Diamedix Corporation |
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