meddevicedb.com FDA Device Reference

MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT

K913441 Class II Traditional
Decision Date
1991-10-21
Sponsor / Applicant
Mri Devices Corp.

Technical Specification

510(k) Submission ID K913441
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 1991-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT received FDA 510(k) clearance under submission number K913441, 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 1991-10-21.

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.