Medical Device Recalls
-
1 result found
510(K) Number: K072288 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pathfast D-Dimer, Reference number: PF1051-KUS | 2 | 11/21/2016 | Lsi Medience Corporation |
-