Inolase 2002, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071943 | SERENITY PRO PSF SYSTEM | GEX | 2007-08-10 | View |
| 510(k) | K062589 | SERENITY PSF (PNEUMATIC SKIN FLATTENING) SYSTEM | GEX | 2006-11-30 | View |
No matching devices.
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