Medical Device Recalls
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1 result found
510(K) Number: K080391 |
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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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PURE OXYGEN CONCENTRATOR, CHAD Drive, Models CH5000 and CH5000S | 2 | 01/24/2018 | Inovo, Inc |
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