510(k) K220800

Venue Go by GE Medical Systems Ultrasound And Primary Care Diagnostics — Product Code IYN

K220800 is an FDA 510(k) premarket notification submitted by GE Medical Systems Ultrasound And Primary Care Diagnostics for the device "Venue Go". The FDA issued a decision of Substantially Equivalent on Jun 21, 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.