510(k) K242770

EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG by DRTECH Corporation — Product Code MQB

K242770 is an FDA 510(k) premarket notification submitted by DRTECH Corporation for the device "EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG". The FDA issued a decision of Substantially Equivalent on March 20, 2025. 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.