Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K853585 |
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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 JF-140F duodenoscopes (Model NumberJF-140F) | 2 | 06/21/2018 | Olympus Corporation of the Americas |
Olympus JF-160F duodenoscopes (Model NumberJF-160F) | 2 | 06/21/2018 | Olympus Corporation of the Americas |
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