Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K080403 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This instrument has been... | 2 | 02/04/2016 | Olympus Corporation of the Americas |
EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has been designed to be u... | 2 | 09/22/2015 | Olympus America Inc. |
-