Medical Device Recalls
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1 result found
510(K) Number: K973030 |
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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 Immunodiagnostic Products CK-MB Calibrators, REF 128 6293, IVD, Ortho-Clinical Diagnostics H... | 3 | 05/17/2013 |
FEI # 1000136573 Ortho-Clinical Diagnostics |
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