FDA 510(k) Applications Submitted by PHOTOMEDEX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K082721 09/17/2008 LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS PHOTOMEDEX, INC.
K040234 02/02/2004 LASERPRO CO2 CARBON DIOXIDE LASER SYSTEM PHOTOMEDEX, INC.
K040294 02/06/2004 LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980 PHOTOMEDEX, INC.


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