Medical Device Recalls
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1 result found
510(K) Number: K221557 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V. | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
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