VCTS 700S System

FDA 510(k) K881021 · Vistech Consultants, Inc.

Substantially Equivalent

510(k) numberK881021

Submission

Device name
VCTS 700S System
Applicant
Vistech Consultants, Inc.
Dayton, OH, US
Received
March 10, 1988
Decision date
April 1, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HOX – Chart, Visual Acuity
Device class
Class I (low risk)
Regulation
21 CFR 886.1150
Specialty
Ophthalmic

Other 510(k)s with product code HOX

510(k)DeviceApplicantDecision
K100095Central Vision Analyzer Model 1000HOX · Abbreviated Vimetrics,Llc.05/10/2010SE
K944156Heine Lambda 100HOX · Traditional Heine USA , Ltd.01/12/1995SE
K881971Occu-Tech Vision TestHOX · Traditional Applied Vision Concepts, Inc.11/25/1988SE
K883337PL 20/20 Infant Vision TesterHOX · Traditional Optimed Technologies, Inc.10/31/1988SE
K882634Visual Contrast Sensiti., Potential Acuity&GlareHOX · Traditional Vistech Consultants, Inc.07/15/1988SE
K881358PG Consen Contrast Sensitivity Testing ProgramHOX · Traditional Neuroscientific Corp.06/27/1988SE
K881059MCT 8000 (Multi-Vision Contrast Tester)HOX · Traditional Vistech Consultants, Inc.04/04/1988SE
K881023VCTS 6500 SystemHOX · Traditional Vistech Consultants, Inc.04/01/1988SE
K881022VCTS Marketing Program SystemHOX · Traditional Vistech Consultants, Inc.04/01/1988SE
K880647Adult Perceptual Motor Puzzles (5331-01)HOX · Traditional Fred Sammons, Inc.04/01/1988SE

More from Fred Sammons, Inc.

510(k)DeviceDecision
K882634Visual Contrast Sensiti., Potential Acuity&GlareHOX · Traditional 07/15/1988SE
K881059MCT 8000 (Multi-Vision Contrast Tester)HOX · Traditional 04/04/1988SE
K881023VCTS 6500 SystemHOX · Traditional 04/01/1988SE
K881022VCTS Marketing Program SystemHOX · Traditional 04/01/1988SE
K853481Vistech VCTS Glare TesterHOX · Traditional 10/29/1985SE
K840255Vistech VCTS 6000HOX · Traditional 04/13/1984SE

Questions and answers

When was VCTS 700S System cleared by the FDA?

VCTS 700S System (K881021) received a 510(k) decision of Substantially Equivalent on April 1, 1988, 22 days after the submission was received.

What is the product code of K881021?

The FDA product code is HOX – Chart, Visual Acuity, a Class I (low risk) device regulated under 21 CFR 886.1150.