Medical Device Recalls
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1 result found
510(K) Number: K090539 |
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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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Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for ... | 1 | 09/09/2022 | Philips Respironics, Inc. |
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