Medical Device Recalls
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1 result found
510(K) Number: K122715 |
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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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ResMed Stellar, Non-invasive/invasive ventilators, Model: 100, 150 | 1 | 02/07/2020 | ResMed Ltd. |
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