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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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