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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