Cleared Traditional

STENTOR, PAGEVIEW

K992698 · Stentor, Inc. · Radiology

Oct 1999

Decision

75d

Days

Class 1

Risk

About This 510(k) Submission

K992698 is an FDA 510(k) clearance for the STENTOR, PAGEVIEW, a System, Digital Image Communications, Radiological (Class I — General Controls, product code LMD), submitted by Stentor, Inc. (San Leandro, US). The FDA issued a Cleared decision on October 25, 1999, 75 days after receiving the submission on August 11, 1999. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2020.

Submission Details

510(k) Number	K992698 FDA.gov
FDA Decision	Cleared SESE
Date Received	August 11, 1999
Decision Date	October 25, 1999
Days to Decision	75 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	Summary PDF

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.