Medical Device Recalls
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1 result found
510(K) Number: K203749 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning.... | 2 | 07/20/2022 | Ambu Inc. |
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