Medical Device Recalls
-
|
1 result found
510(K) Number: K143651 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) ... | 1 | 04/02/2016 |
FEI # 2023365 Focus Diagnostics Inc |
-







