Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K172298 |
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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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Olympus URETERO-RENO FIBERSCOPE Model: URF-P6 | 2 | 06/13/2022 | Olympus Corporation of the Americas |
Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R | 2 | 06/13/2022 | Olympus Corporation of the Americas |
Uretero-reno fiberscope URF-P6 | 2 | 07/20/2018 | Olympus Corporation of the Americas |
Uretero-reno fiberscope URF-P6RP6 | 2 | 07/20/2018 | Olympus Corporation of the Americas |
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