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FDA 510(k) Applications Submitted by SYNERON CANDELA CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170597
02/28/2017
PicoWay Laser System
Syneron Candela Corporation
K160607
03/02/2016
PicoWay Laser System
SYNERON CANDELA CORPORATION
K161043
04/13/2016
Profound System
SYNERON CANDELA CORPORATION
K162454
09/01/2016
PicoWay Laser System
SYNERON CANDELA CORPORATION
K153527
12/09/2015
PicoWay Laser System
SYNERON CANDELA CORPORATION
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