510(k) K223267

SKR 3000 by Konica Minolta, Inc. — Product Code MQB

K223267 is an FDA 510(k) premarket notification submitted by Konica Minolta, Inc. for the device "SKR 3000". The FDA issued a decision of Substantially Equivalent on November 17, 2022. 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. Konica Minolta, Inc. has at least 10 other 510(k) clearances on record.