FDA 510(k) Applications for Medical Device Product Code "JSI"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K070691 | BECTON, DICKINSON & CO. | BBL CHROMAGAR 0157 | 11/20/2007 |
K974428 | NOVAMED LTD. | DIPSTREAK | 07/30/1998 |