meddevicedb.com FDA Device Reference

MODEL #QSC-200, 20CM. QUADRATURE SHOULDER COIL

K922000 Class II Traditional
Decision Date
1992-07-28
Sponsor / Applicant
Mri Devices Corp.

Technical Specification

510(k) Submission ID K922000
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 1992-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL #QSC-200, 20CM. QUADRATURE SHOULDER COIL received FDA 510(k) clearance under submission number K922000, sponsored by Mri Devices Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1992-07-28.

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.