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Home » Syneron Files With FDA for 510(k) of VelaSmooth in U.S.
Syneron Files With FDA for 510(k) of VelaSmooth in U.S.
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.
KEYWORDS FDAnews Device Daily Bulletin
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