meddevicedb.com FDA Device Reference

R190/R191 LCD Monitor

K183494 Class II Traditional
Decision Date
2019-04-05
Sponsor / Applicant
Nanjing Jusha Display Technology Co., Ltd.

Technical Specification

510(k) Submission ID K183494
Product Code PGY
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2019-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

R190/R191 LCD Monitor received FDA 510(k) clearance under submission number K183494, sponsored by Nanjing Jusha Display Technology 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 2019-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code PGY and 21 CFR 892.2050, within the Radiology review panel as a Class II device.