Medical Device Recalls
-
1 result found
510(K) Number: K190219 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
MOL3650 Simplexa VZV Direct - Product Usage: is intended for use on the LIAISON MDX instrument for t... | 2 | 07/10/2020 | DiaSorin Molecular LLC |
-