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FDA 510(k) Applications Submitted by QUICKLASE LIMITED
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100474
02/18/2010
QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W
QUICKLASE LIMITED
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