Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K192793 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Colonoscope, Model Number PCF-H190TL. | 2 | 02/29/2024 | Olympus Corporation of the Americas |
| Colonoscope, Model Number PCF-HQ190L. | 2 | 02/29/2024 | Olympus Corporation of the Americas |
| Colonoscope-indicated for use within the lower digestive tract (including the anus, rectum, sigmoid ... | 2 | 11/17/2023 | Aizu Olympus Co., Ltd. |
-







