Medical Device Recalls
-
|
1 result found
510(K) Number: K052884 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Toshiba-Interventional Angiography System, Infinix i, Model DFP-8000D, equiped with Digital Radiogr... | 2 | 11/27/2007 |
FEI # 2020563 Toshiba American Med Sys Inc |
-







