Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K193182 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system cent... | 2 | 03/22/2021 | Olympus Corporation of the Americas |
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V | 2 | 08/28/2023 | Olympus Corporation of the Americas |
-