Medical Device Recalls
-
|
1 result found
510(K) Number: K900802 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| CD4 (SK3), FITC; Contains CD4 FITC with gelatin and 0.1% sodium Azide. Catalog number 340133 in... | 3 | 09/24/2015 |
FEI # 2916837 Becton, Dickinson and Company, BD Biosciences |
-







