Medical Device Recalls
-
1 result found
510(K) Number: K171441 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ARIES C. difficile Assay , REF 50-10018, UDI # 00840487100059 | 2 | 08/15/2019 | Luminex Corporation |
-