510(k) K163572

LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source by Lv Liberty Vision Corp. — Product Code KXK

K163572 is an FDA 510(k) premarket notification submitted by Lv Liberty Vision Corp. for the device "LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source". The FDA issued a decision of Substantially Equivalent on March 15, 2017. The device falls under product code KXK (Source, Brachytherapy, Radionuclide), a Class II device regulated under 21 CFR 892.5730.