510(k) K131958

BAUSCH & LOMB INJECTOR SYSTEM by Bausch & Lomb — Product Code MSS

K131958 is an FDA 510(k) premarket notification submitted by Bausch & Lomb for the device "BAUSCH & LOMB INJECTOR SYSTEM". The FDA issued a decision of Substantially Equivalent on January 9, 2014. The device falls under product code MSS (Folders And Injectors, Intraocular Lens (Iol)), a Class I device regulated under 21 CFR 886.4300. Bausch & Lomb has at least 10 other 510(k) clearances on record.