FDA 510(k) Applications Submitted by GIAN FRANCO BERNABEI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K965256 | 08/16/1996 | DMS-1000C DERMOABRADER | MATTIOLI ENGINEERING, SRL |
| K100053 | 01/08/2010 | MATTIOLI PULSE TWO/THREE PLUS FAMILY | MATTIOLI ENGINEERING CORP. |
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