FDA 510(k) Applications Submitted by RICHARD ALBRIGHT

FDA 510(k) Number Submission Date Device Name Applicant
K050070 01/12/2005 K-LASER, MODELS 3,4,4D,6D ELTECH, S.R.L.
K120604 02/28/2012 K-LASER ELTECH S.R.L
K091497 05/20/2009 K-LASER K-1200, MODEL 12 W ELTECH, S.R.L.


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