FDA 510(k) Applications for Medical Device Product Code "NWG"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K072135 | KRONUS MARKET DEVELOPMENT ASSOCIATES, INC. | KRONUS GAD AUTOANTIBODY ELISA ASSAY KIT | 11/07/2007 |
K051061 | KRONUS MARKET DEVELOPMENT ASSOCIATES, INC. | KRONUS GLUTAMIC ACID DECARBOXYLASE ANTIBODY KIT | 11/04/2005 |