Medical Device Recalls
-
1 result found
510(K) Number: K072189 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
PATHFAST NTproBNP Catalog Number: PF1061-KUS PATHFAST® NTproBNP is a product for in-vitro diagn... | 2 | 09/17/2018 | Polymedco, Inc.,/Polymedco Cancer Diagnostic Products, Llc |
-