Medical Device Recalls
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1 result found
510(K) Number: K983875 |
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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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| VITROS CA 125 II Calibrators For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic S... | 2 | 12/17/2013 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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