510(k) K172082

S60 Series Digital Color Doppler Ultrasound System by Sonoscape Medical Corp. — Product Code IYN

K172082 is an FDA 510(k) premarket notification submitted by Sonoscape Medical Corp. for the device "S60 Series Digital Color Doppler Ultrasound System". The FDA issued a decision of Substantially Equivalent on September 21, 2017. 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.