Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K955023 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| IQecg IQdevices SDK, Part Numbers: 4-100-1403, Software Version 8.3.2 Product Usage: IQecg is to... | 2 | 07/14/2011 |
FEI # 2081230 Brentwood Medical Technology Corp |
| IQecg IQiC Interface, Part Numbers: 4-100-1407, Software Version 6.0 IQecg is to be used, under t... | 2 | 07/14/2011 |
FEI # 2081230 Brentwood Medical Technology Corp |
| IQecg IQmanager Diagnostic Workstation, Part Numbers: 4-100-1200, Software Version 8.0.1, 8.3, 8.3.1... | 2 | 07/14/2011 |
FEI # 2081230 Brentwood Medical Technology Corp |
-







