Medical Device Recalls
-
1 result found
510(K) Number: K955440 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic use with the IMMULITE 2000 Systems... | 2 | 04/19/2017 | Siemens Healthcare Diagnostics, Inc. |
-