meddevicedb.com FDA Device Reference

SMT-50X/H MAGNETIC RESONANCE IMAGING SYSTEM

K923984 Class II Traditional
Decision Date
1993-03-16
Sponsor / Applicant
Shimadzu Medical Systems

Technical Specification

510(k) Submission ID K923984
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 1993-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMT-50X/H MAGNETIC RESONANCE IMAGING SYSTEM received FDA 510(k) clearance under submission number K923984, sponsored by Shimadzu Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1993-03-16.

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.