Medical Device Recalls
-
1 result found
510(K) Number: K072521 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Vue Optic Visualization Source, Flexor Vue Deflecting Endoscopic System, Endoscope, Fiber Optic, Sup... | 2 | 06/05/2017 | Cook Inc. |
-