Energist, Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
Advertisement
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K132754 | NEOGEN PSR SYSTEM | GEI | 2013-12-12 | View |
| 510(k) | K082825 | ENERGIST ULTRAPLUS VARIABLE PULSED LIGHT (VPL) SYSTEM | GEX | 2009-02-06 | View |
| 510(k) | K060216 | ENERGIST ULTRA VPL INTENSE PULSE LIGHT SYSTEM | GEX | 2006-03-16 | View |
No matching devices.
Advertisement