Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K201339 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I | 1 | 10/06/2025 | NOXBOX LTD |
| NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I | 1 | 10/06/2025 | NOXBOX LTD |
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