meddevicedb.com FDA Device Reference

MODEL 475 - 8 CHANNEL T/R PHASED ARRAY LOWER EXTREMITY COIL

K040640 Class II Traditional
Decision Date
2004-03-22
Sponsor / Applicant
Igc-Medical Advances, Inc.

Technical Specification

510(k) Submission ID K040640
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2004-03-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 475 - 8 CHANNEL T/R PHASED ARRAY LOWER EXTREMITY COIL received FDA 510(k) clearance under submission number K040640, sponsored by Igc-Medical Advances, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2004-03-22.

Classification & Regulation

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