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FDA 510(k) Applications for Medical Device Product Code "GFD"
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| 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 |