Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K221557 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Visera Hysterovideoscope Olympus HYF Type V | 2 | 08/29/2023 | Olympus Corporation of the Americas |
| Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V. | 2 | 11/17/2023 | Aizu Olympus Co., Ltd. |
-







