meddevicedb.com FDA Device Reference

DIGITAL IMAGE PROCESSOR FP-2C

K850080 Class II Traditional
Decision Date
1985-04-19
Sponsor / Applicant
Eigen Video

Technical Specification

510(k) Submission ID K850080
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 1985-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGITAL IMAGE PROCESSOR FP-2C received FDA 510(k) clearance under submission number K850080, sponsored by Eigen Video. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1985-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.