Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K963033 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Olympus Bronchovideoscope, Models BF-3C160. | 2 | 08/31/2023 | Olympus Corporation of the Americas |
Bronchovideoscope BF-P240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchovidescope BF-1T240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchovideoscope BF-240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
-