Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K170924 |
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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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AirFit F30 Full Face Mask and User Guide | 1 | 12/21/2023 | ResMed Ltd. |
AirFit F20 Full Face Mask and User Guide | 1 | 12/21/2023 | ResMed Ltd. |
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