Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K070983 |
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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-UC180F | 2 | 09/29/2018 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus Bronchovideoscope, Models BF-UC180F & BF-UC190F. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspirat... | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
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