Medical Device Recalls
-
|
1 result found
510(K) Number: K896493 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Mycobacterium Tuberculosis Complex Culture Identification Test, 2860. | 1 | 03/10/2011 | Gen-Probe Inc |
-







