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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K171696
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device 1 06/09/2023 NOXBOX LTD
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