Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133868 |
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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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Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive h... | 2 | 02/03/2016 | Resmed Corporation |
Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator. | 2 | 06/10/2015 | ResMed Ltd. |
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