Medical Device Recalls
-
|
1 result found
510(K) Number: K132261 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| GE Healthcare, Discovery XR656P/N 5374989/5397837 is intended to generate digital radiographic image... | 2 | 08/20/2014 |
FEI # 2126677 GE Healthcare, LLC |
-







