Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K112680 |
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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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| Colonoscope, Model Number CF-HQ190L. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Colonoscope, Model Number PCF-H190L. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Colonoscope, Model Number CF-HQ190I. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esopha... | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| EVIS EXERA III Gastrointestinal Videoscope | 2 | 11/09/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
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