Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K190533 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mojo 2 Full Face AAV Non Vented Mask, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
| Mojo 2 Full Face Non Vented Mask, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
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