Medical Device Recalls
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1 result found
510(K) Number: K203193 |
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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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| Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver ... | 1 | 07/22/2022 |
FEI # 3006260740 Bard Access Systems, Inc. |
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