Medical Device Recalls
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1 result found
510(K) Number: K131895 |
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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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Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US | 2 | 05/15/2024 | Fisher & Paykel Healthcare, Ltd. |
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