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FDA 510(k) Applications Submitted by CURAE'LASE INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130168
01/24/2013
CL10009 IR LASER
CURAE'LASE INC.
K053201
11/16/2005
CURAE'LASE CL1000 IR LASER SYSTEM
CURAE'LASE INC.
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