Medical Device Recalls
-
|
1 result found
510(K) Number: K103385 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Hologics SecurView DX workstation, software version 7.3.0 intended for viewing mammography images ... | 2 | 04/05/2012 |
FEI # 1221300 Hologic, Inc. |
-







