510(k) K240206

Venue Sprint by GE Medical Systems Ultrasound and Primary Care Diagnostics — Product Code IYN

K240206 is an FDA 510(k) premarket notification submitted by GE Medical Systems Ultrasound and Primary Care Diagnostics for the device "Venue Sprint". The FDA issued a decision of Substantially Equivalent on June 10, 2024. 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 at least 10 other 510(k) clearances on record.