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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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