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KODAK DIGITAL SCIENCE QUALITY CONTROL WORKSTATION (QCW)

K974107 Class I Traditional
Decision Date
1998-01-21
Sponsor / Applicant
Eastman Kodak Company

Technical Specification

510(k) Submission ID K974107
Product Code LMD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2020
Decision Date 1998-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KODAK DIGITAL SCIENCE QUALITY CONTROL WORKSTATION (QCW) received FDA 510(k) clearance under submission number K974107, sponsored by Eastman Kodak Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1998-01-21.

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.