FDA 510(k) Applications Submitted by IDS, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K171079 04/11/2017 Q-Switched Nd:YAG Laser System IDS, Ltd.
K181868 07/12/2018 SHINY RPL System IDS, Ltd.
K180036 01/05/2018 SMAXEL CO2 Surgical Laser System IDS, LTD.


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