Medical Device Recalls
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1 result found
510(K) Number: K102465 |
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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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DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, Omni... | 1 | 07/13/2021 | Philips Respironics, Inc. |
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