Medical Device Recalls
-
1 result found
510(K) Number: K111822 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Stago IVD, Liquid Anti-Xa, NDC 3607450003116. The STA - Liquid Anti-Xa kits are intended for use ... | 3 | 09/16/2014 | Diagnostica Stago, Inc. |
-