Medical Device Recalls
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1 result found
510(K) Number: K190875 |
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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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The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled TDC Vitrectom... | 2 | 08/12/2021 | Dutch Ophthalmic USA, Inc. |
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