Medical Device Recalls
-
|
1 result found
510(K) Number: K012820 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| ST-AIA PACK cTnI 2nd Gen; Part Number: 025205 Assay, Cardiac Marker | 2 | 06/05/2018 | Tosoh Bioscience Inc |
-







