FDA 510(k) Applications Submitted by GENERAL PROJECT S.R.L.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062312 | 08/08/2006 | AXIOM PULSED LIGHT SYSTEM | GENERAL PROJECT S.R.L. |
| K091615 | 06/03/2009 | MED CONTOUR | GENERAL PROJECT S.R.L. |
| K051508 | 06/07/2005 | MED FLASH II INTENSE PULSED LIGHT SYSTEM. | GENERAL PROJECT S.R.L. |
| K053041 | 10/27/2005 | MED SCULPT | GENERAL PROJECT S.R.L. |
| K161502 | 06/01/2016 | MC1 Plus | GENERAL PROJECT S.R.L. |
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