510(k) K183212

Nexus DR Digital X-ray Imaging System with stitching by Varex Imaging Corporation — Product Code MQB

K183212 is an FDA 510(k) premarket notification submitted by Varex Imaging Corporation for the device "Nexus DR Digital X-ray Imaging System with stitching". The FDA issued a decision of Substantially Equivalent on December 7, 2018. The device falls under product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)), a Class II device regulated under 21 CFR 892.1680. Varex Imaging Corporation has at least 6 other 510(k) clearances on record.