Medical Device Recalls
-
|
1 result found
510(K) Number: K091498 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Vitrea 5.1. Vitrea fX 3.0, Vitrea Enterprise Suite 1.2 with the licensing of CT lung or CT Colon. | 2 | 05/13/2010 |
FEI # 3001654007 Vital Images, Inc. |
-







