510(k) K023750

CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G by Canon USA, Inc. — Product Code MQB

K023750 is an FDA 510(k) premarket notification submitted by Canon USA, Inc. for the device "CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G". The FDA issued a decision of Substantially Equivalent on November 22, 2002. 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. Canon USA, Inc. has at least 10 other 510(k) clearances on record.