Medical Device Recalls
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1 result found
510(K) Number: K912120 |
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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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URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope | 2 | 02/24/2017 | Olympus Corporation of the Americas |
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