Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K092238 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Agfa Computed Radiography Systems with DX-G Digitizer. DX-G Digitizers haved the same intended us... | 2 | 01/11/2012 | AGFA Corp. |
DX-G Digitizer, manufactured by Agfa-Gevart NV, Mortsel, Belgium. | 2 | 11/26/2010 | AGFA Corp. |
-