Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K170558 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Revogene, Catalog no. 610210. IVD test instrument | 2 | 07/28/2022 | Meridian Bioscience Inc |
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. ... | 2 | 03/30/2022 | Meridian Bioscience Inc |
-