510(k) K223124

EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG by DRTECH Corporation — Product Code MQB

K223124 is an FDA 510(k) premarket notification submitted by DRTECH Corporation for the device "EXPD 86P, EXPD 86PG, EXPD 129P, EXPD 129PG". The FDA issued a decision of Substantially Equivalent on November 18, 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. DRTECH Corporation has at least 10 other 510(k) clearances on record.