Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K060256 |
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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| Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N); (2) Access 2 Immunoassay ... | 2 | 03/15/2023 |
FEI # 2122870 Beckman Coulter, Inc. |
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