meddevicedb.com FDA Device Reference

NeuViz Prime Multi-slice CT Scanner System

K171201 Class II Traditional
Decision Date
2017-09-13
Sponsor / Applicant
Neusoft Medical Systems Co., Ltd.

Technical Specification

510(k) Submission ID K171201
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2017-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NeuViz Prime Multi-slice CT Scanner System received FDA 510(k) clearance under submission number K171201, sponsored by Neusoft Medical Systems Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.