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MODEL FORTY ULTRA COMPACT VIDEO IMAGER

K940332 Class II Traditional
Decision Date
1994-06-08
Sponsor / Applicant
International Imaging Electronics

Technical Specification

510(k) Submission ID K940332
Product Code LMC
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2040
Decision Date 1994-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL FORTY ULTRA COMPACT VIDEO IMAGER received FDA 510(k) clearance under submission number K940332, 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 1994-06-08.

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.