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MP3000 SERIES II COMPACT VIDEO IMAGER

K900900 Class II Traditional
Decision Date
1990-04-30
Sponsor / Applicant
International Imaging Electronics

Technical Specification

510(k) Submission ID K900900
Product Code LMC
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2040
Decision Date 1990-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MP3000 SERIES II COMPACT VIDEO IMAGER received FDA 510(k) clearance under submission number K900900, 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 1990-04-30.

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.