meddevicedb.com FDA Device Reference

S60 Elite Series/S70 Series Digital Color Doppler Ultrasound System

K201059 Class II Traditional
Decision Date
2020-07-30
Sponsor / Applicant
Sonoscape Medical Corp.

Technical Specification

510(k) Submission ID K201059
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2020-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S60 Elite Series/S70 Series Digital Color Doppler Ultrasound System received FDA 510(k) clearance under submission number K201059, sponsored by Sonoscape Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2020-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.