meddevicedb.com FDA Device Reference

MULTI FORMAT VIDEO IMAGER 600 PLUS

K904363 Class II Traditional
Decision Date
1990-11-13
Sponsor / Applicant
International Imaging Electronics

Technical Specification

510(k) Submission ID K904363
Product Code LMC
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2040
Decision Date 1990-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTI FORMAT VIDEO IMAGER 600 PLUS received FDA 510(k) clearance under submission number K904363, sponsored by International Imaging Electronics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1990-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code LMC and 21 CFR 892.2040, within the Radiology review panel as a Class II device.