Cleared Traditional

IMAGEQUEST

K974707 · Visual Med, Inc. · Radiology

Jul 1998

Decision

227d

Days

Class 1

Risk

About This 510(k) Submission

K974707 is an FDA 510(k) clearance for the IMAGEQUEST, a System, Digital Image Communications, Radiological (Class I — General Controls, product code LMD), submitted by Visual Med, Inc. (Ft. Mill, US). The FDA issued a Cleared decision on July 31, 1998, 227 days after receiving the submission on December 16, 1997. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2020.

Submission Details

510(k) Number	K974707 FDA.gov
FDA Decision	Cleared SESE
Date Received	December 16, 1997
Decision Date	July 31, 1998
Days to Decision	227 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	Statement

Device Classification

Product Code	LMD — System, Digital Image Communications, Radiological
Device Class	Class I — General Controls
CFR Regulation	21 CFR 892.2020
Definition	A Medical Image Communications Device Provides Electronic Transfer Of Medical Image Data Between Medical Devices. It May Include A Physical Communications Medium, Modems, Interfaces, And A Communications Protocol. It May Provide Simple Image Review Software Functionality For Medical Image Processing And Manipulation, Such As Grayscale Window And Level, Zoom And Pan, User Delineated Geometric Measurements, Compression, Or User Added Image Annotations. The Device Does Not Perform Advanced Image Processing Or Complex Quantitative Functions.