Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K100584 |
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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-H180AL. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Colonoscope, Model Number PCF-H180AL. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Colonoscope, Model Number CF-Q180AL. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Colonoscope, Model Number PCF-Q180AL. | 2 | 02/29/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within the lower digestive trac... | 2 | 02/13/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Colonovideoscope Model CF-H180AL | 2 | 06/21/2022 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are intended for use in endos... | 2 | 03/12/2019 |
FEI # 2429304 Olympus Corporation of the Americas |
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