meddevicedb.com FDA Device Reference

SonoVision Ultrasound Imaging System

K192388 Class II Abbreviated
Decision Date
2020-03-12
Sponsor / Applicant
Tissue Differentiation Intelligence, LLC

Technical Specification

510(k) Submission ID K192388
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2020-03-12
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SonoVision Ultrasound Imaging System received FDA 510(k) clearance under submission number K192388, sponsored by Tissue Differentiation Intelligence, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2020-03-12.

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.