FDA 510(k) Applications Submitted by AESTHERA CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062048 | 07/20/2006 | AESTHERA PHOTOPNEUMATIC (PPX) SYSTEM | AESTHERA CORPORATION |
| K041554 | 06/10/2004 | AIP INTENSE PULSED LIGHT SYSTEM | AESTHERA CORPORATION |
| K083730 | 12/16/2008 | ISOLAZ | AESTHERA CORPORATION |
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