Medical Device Recalls
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1 result found
510(K) Number: K192397 |
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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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TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: ... | 2 | 10/20/2023 | Acclarent, Inc. |
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