Medical Device Recalls
-
|
1 result found
510(K) Number: K983359 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Immunoglobulin A is an in vitro diagnostic assay for the quantitative determination of immunoglobul... | 2 | 07/19/2019 |
FEI # 1628664 Abbott Laboratories, Inc |
-







