510(k) K893750

MRT-50A MOBILE by Toshiba Medical Systems — Product Code LNH

K893750 is an FDA 510(k) premarket notification submitted by Toshiba Medical Systems for the device "MRT-50A MOBILE". The FDA issued a decision of Substantially Equivalent on August 9, 1989. The device falls under product code LNH (System, Nuclear Magnetic Resonance Imaging), a Class II device regulated under 21 CFR 892.1000. Toshiba Medical Systems has at least 10 other 510(k) clearances on record.