FDA 510(k) Applications Submitted by MIKI KOLTON

FDA 510(k) Number Submission Date Device Name Applicant
K070690 03/13/2007 THE LIFE VESSEL COTTONWOOD VESSEL CORPORATION
K082969 10/06/2008 LUMINEX INFRARED LAMP SYSTEM MEDICAL LASER SYSTEMS INC
K063574 11/29/2006 LUMINEX LL LASER SYSTEM MEDICAL LASER SYSTEMS INC


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