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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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