Medical Device Recalls
-
|
1 result found
510(K) Number: K992432 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| BacT/ALERT® FN Culture Bottles, Product Number 259793 | 2 | 08/22/2007 | bioMerieux, Inc. |
-







