Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K221683 |
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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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| Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE | 2 | 01/09/2024 |
FEI # 3002808148 Shirakawa Olympus Co., Ltd. |
| Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope | 2 | 01/09/2024 |
FEI # 3002808148 Shirakawa Olympus Co., Ltd. |
| Model No. CYF-V2, VISERA Cysto-Nephro Videoscope | 2 | 01/09/2024 |
FEI # 3002808148 Shirakawa Olympus Co., Ltd. |
| Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE | 2 | 01/09/2024 |
FEI # 3002808148 Shirakawa Olympus Co., Ltd. |
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