Aesthera Corporation
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K083730 | ISOLAZ | GEX | 2009-01-09 | View |
| 510(k) | K062048 | AESTHERA PHOTOPNEUMATIC (PPX) SYSTEM | GEX | 2006-09-07 | View |
| 510(k) | K041554 | AIP INTENSE PULSED LIGHT SYSTEM | GEX | 2005-04-27 | View |
No matching devices.
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