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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