FDA 510(k) Applications Submitted by ANDREW J BERRY

FDA 510(k) Number Submission Date Device Name Applicant
K062871 09/25/2006 LUMACARE LC-122M NON-COHERENT LIGHT SOURCE LYNTON LASERS LIMITED
K072048 07/25/2007 LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE LYNTON LASERS LIMITED
K063427 11/13/2006 LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM LYNTON LASERS LIMITED


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