FDA 510(k) Applications Submitted by CURELIGHT LTD

FDA 510(k) Number Submission Date Device Name Applicant
K030338 01/31/2003 ICLEAR PHOTOTHERAPY SYSTEM, MODEL FGCM0002 CURELIGHT LTD
K032383 08/01/2003 MULTICLEAR MULTIWAVELENGTH TARGETED PHOTOTHERAPY SYSTEM CURELIGHT LTD
K033183 10/01/2003 RECLEAR PHOTOTHERAPY SYSTEM, MODEL FGCM0012 CURELIGHT LTD
K013623 11/05/2001 CLEARLIGHT PHOTOTHERAPHY SYSTEM, MODEL CL 420 CURELIGHT LTD
K041569 06/10/2004 CLEAR100 PHOTOTHERAPY SYSTEM, MODEL FGCM0002 CURELIGHT LTD
K041994 07/23/2004 MULTICLEAR XL MULTIWAVELENGTH TARGETED PHOTOTHERAPY SYSTEM CURELIGHT LTD


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