Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K792035 |
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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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Bivona Uncuffed Wire Endotracheal Tubes, | 2 | 10/27/2021 | Smiths Medical ASD Inc. |
Bivona Aire-Cuf Endotracheal Tube | 2 | 10/27/2021 | Smiths Medical ASD Inc. |
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