Medical Device Recalls
-
|
1 result found
510(K) Number: K080635 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid, qualitative detection of drugs of... | 2 | 05/16/2013 |
FEI # 1050155 Medtox Diagnostics Inc |
-







