Medical Device Recalls
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1 result found
510(K) Number: K111521 |
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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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| WAVES WCM Kidney Cassette Module | 2 | 04/27/2022 |
FEI # 2123774 Waters Medical Systems LLC |
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