Medical Device Recalls
-
1 result found
510(K) Number: K192050 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553 | 2 | 01/04/2023 | Biomerieux Inc |
-