Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K983070 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Abbott ARCHITECT Creatine Kinase, IVD, REF 7D63-21. | 2 | 03/30/2019 | Abbott Laboratories, Inc |
| Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341. | 2 | 03/30/2019 | Abbott Laboratories, Inc |
| Abbott Clinical Chemistry Creatine Kinase, Model LN 7D63-30, Lot Number: 52044HW00; Expires October ... | 2 | 03/19/2008 | Abbott Laboratories Inc. |
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