FDA 510(k) Applications Submitted by JM SYSTEM CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K100098 01/13/2010 PLASMALIPO/PLASMA D30 LSER SURGICAL DEVICE JM SYSTEM CO., LTD.
K100590 03/02/2010 EDGE CO2 LASER SYSTEM JM SYSTEM CO., LTD.


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