Medical Device Recalls
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1 result found
510(K) Number: K123979 |
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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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Quattro Air FFM MED AMER, Product Code: 62702, full face mask for use with active-exhaust-valve v... | 2 | 08/16/2016 | Resmed Corporation |
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