Medical Device Recalls
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1 result found
510(K) Number: K060475 |
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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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| Ultrasonic Bronchoscope BF-UC160F-OL8 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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