Medical Device Recalls
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1 result found
510(K) Number: K171696 |
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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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NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device | 1 | 06/09/2023 | NOXBOX LTD |
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