www.fdanews.com/articles/68866-syneron-files-with-fda-for-510-k-of-velasmooth-in-u-s
Syneron Files With FDA for 510(k) of VelaSmooth in U.S.
February 17, 2005
Syneron Medical, a developer and marketer of ELOS combined-energy medical aesthetic devices, announced that it has filed a 510(k) application with the FDA for marketing clearance of its VelaSmooth system in the U.S.