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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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