Medical Device Recalls
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1 result found
510(K) Number: K060751 |
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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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Inovo Single Luman Conserver Product Usage: This device is intended to regulate the flow of oxyg... | 2 | 07/29/2019 | Inovo, Inc |
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