510(k) K220619

Vivid S60N, Vivid S70N by GE Medical Systems Ultrasound And Primary Care Diagnostics — Product Code IYN

K220619 is an FDA 510(k) premarket notification submitted by GE Medical Systems Ultrasound And Primary Care Diagnostics for the device "Vivid S60N, Vivid S70N". The FDA issued a decision of Substantially Equivalent on Jul 15, 2022. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550. GE Medical Systems Ultrasound And Primary Care Diagnostics has 82 other 510(k) clearances on record.