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FDA 510(k) Applications Submitted by ELTECH, S.R.L.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050070
01/12/2005
K-LASER, MODELS 3,4,4D,6D
ELTECH, S.R.L.
K091497
05/20/2009
K-LASER K-1200, MODEL 12 W
ELTECH, S.R.L.
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