FDA 510(k) Applications Submitted by MICROLIGHT CORPORATION OF AMERICA

FDA 510(k) Number Submission Date Device Name Applicant
K080786 03/20/2008 ML830TP MICROLIGHT CORPORATION OF AMERICA
K041364 05/21/2004 ML830 LASER SYSTEM MICROLIGHT CORPORATION OF AMERICA
K010175 01/18/2001 MICROLIGHT 830 LASER SYSTEM MICROLIGHT CORPORATION OF AMERICA


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