meddevicedb.com FDA Device Reference

SUPEROPEN 0.23T, MODEL NAM-P023A

K033315 Class II Traditional
Decision Date
2003-10-29
Sponsor / Applicant
Neusoft Digital Medical Systems Co., Ltd.

Technical Specification

510(k) Submission ID K033315
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2003-10-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUPEROPEN 0.23T, MODEL NAM-P023A received FDA 510(k) clearance under submission number K033315, sponsored by Neusoft Digital 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 2003-10-29.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.