Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K060548 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to be used for calibration of th... | 2 | 01/07/2016 | Siemens Healthcare Diagnostics Inc |
Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended to be used for calibration o... | 2 | 01/07/2016 | Siemens Healthcare Diagnostics Inc |
-