Medical Device Recalls
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1 result found
510(K) Number: K062918 |
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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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11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018); 11272VNU 11272VNUK Flexib... | 2 | 05/12/2022 | Karl Storz Endoscopy |
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