FDA 510(k) Applications for Medical Device Product Code "GFD"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K962371 | DSP WORLDWIDE | DERMTOME BLADE | 08/29/1996 |
K965256 | MATTIOLI ENGINEERING, SRL | DMS-1000C DERMOABRADER | 12/09/1996 |