FDA 510(k) Applications for Medical Device Product Code "JII"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K082001 | DIAZYME LABORATORIES | DIAZYME LIQUID STABLE ENZYMATIC LITHIUM ASSAY, MODEL DZ116B | 12/05/2008 |
K033360 | GENERAL ATOMICS | DIAZYME LITHIUM ENZYMATIC ASSAY KIT | 12/23/2003 |