Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K050220 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
BF-Q180-AC EVIS EXERA II Bronchovideoscope, Model No. BF-Q180-AC | 2 | 09/24/2021 | Olympus Corporation of the Americas |
Bronchovideoscope BF-Q180-AC | 2 | 09/29/2018 | Olympus Corporation of the Americas |
-