Medical Device Recalls
-
1 result found
510(K) Number: K912291 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
is a qualitative indirect enzyme immunoassay enzyme-linked immunosorbent assay (ELISA) for the detec... | 3 | 08/23/2018 | Euro Diagnostica AB |
-