FDA 510(k) Applications Submitted by KIM MARSH

FDA 510(k) Number Submission Date Device Name Applicant
K001223 04/17/2000 ACULUX, MODEL AX3001, AX3002 ACULUX
K013511 10/22/2001 XENALIGHT MODELS # AX9125 (100-120V~); # AX9225 (220-240V~) ACULUX, INC.


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