Medical Device Recalls
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1 result found
510(K) Number: K131502 |
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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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| Seattle PAP Plus, MP02260 | 1 | 05/17/2023 |
FEI # 2517967 Draeger Medical, Inc. |
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