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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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