Medical Device Recalls
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1 result found
510(K) Number: K102900 |
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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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| Recirculator 8.0s Disposable Lavage Kit (product code number 8100) , GTIN: 08719992086016. Hyperth... | 1 | 07/23/2021 |
FEI # 3011831824 Eight Medical International BV |
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