Medical Device Recalls
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41 to 41 of 41 Results
510(K) Number: K023984 |
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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| Bronchofiberscope BF-XT40 | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
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