Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K131780 |
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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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Colonoscope, Model Number PCF-H190DL. | 2 | 02/29/2024 | Olympus Corporation of the Americas |
GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE | 2 | 11/29/2023 | Aizu Olympus Co., Ltd. |
PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE | 2 | 11/29/2023 | Aizu Olympus Co., Ltd. |
PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE | 2 | 11/29/2023 | Aizu Olympus Co., Ltd. |
CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE | 2 | 11/29/2023 | Aizu Olympus Co., Ltd. |
GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE | 2 | 11/29/2023 | Aizu Olympus Co., Ltd. |
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