Medical Device Recalls
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1 result found
510(K) Number: K023828 |
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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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"K-ASSAY CRP (3) Calibrator E". This product is an IVD calibrator for use on automated clinical... | 2 | 03/04/2010 | Kamiya Biomedical Company, LLC |
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