meddevicedb.com FDA Device Reference

CD-R STATION AND VRS-2000

K974255 Class I Traditional
Decision Date
1998-01-27
Sponsor / Applicant
Electromed Intl., Ltd.

Technical Specification

510(k) Submission ID K974255
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1998-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CD-R STATION AND VRS-2000 received FDA 510(k) clearance under submission number K974255, sponsored by Electromed Intl., 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 1998-01-27.

Classification & Regulation

This clearance is catalogued under FDA product code LMD and 21 CFR 892.2020, within the Radiology review panel as a Class I device.