510(k) K222596

S90 Exp Series Digital Color Doppler Ultrasound System by Sonoscape Medical Corp. — Product Code IYN

K222596 is an FDA 510(k) premarket notification submitted by Sonoscape Medical Corp. for the device "S90 Exp Series Digital Color Doppler Ultrasound System". The FDA issued a decision of Substantially Equivalent on February 10, 2023. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550. Sonoscape Medical Corp. has at least 10 other 510(k) clearances on record.