Medical Device Recalls
-
1 result found
510(K) Number: K142721 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Nucleic Acid test intended for screening for MRSA/SA. Each kit has 20 tubes. in vitro diagnostic. | 2 | 03/26/2018 | Roche Molecular Systems, Inc. |
-