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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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