About This 510(k) Submission
K190367 is an FDA 510(k) clearance for the Smith & Nephew Tablet Application, a Mobile / Tablet Software Application To Control Settings Of Surgical And Endoscopic Camera (Class II — Special Controls, product code QGY), submitted by Smith & Nephew (Andover, US). The FDA issued a Cleared decision on May 21, 2019, 95 days after receiving the submission on February 15, 2019. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.