FDA.reportPublic FDA data

510(k) K141865

Device
DANA
Applicant
ANTHROTRONIX, INC
510(k) number
K141865
Product code
LQD  
Decision
Substantially Equivalent (SESE)
Decision date
2014-10-15
Date received
2014-07-10
Regulation
510(k) Premarket Notification
Classification name
Recorder, Attention Task Performance
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
Neurology
Device class
U
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
CORINA E LATHAN, PHD, PE
Address
8737 Colesville Rd. Suite L-203 Silver Spring MD US 20910 20910

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LQD  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K173915Test of Variables of Attention (T.O.V.A.)The Tova Company2018-03-22
K170082Test of Variables of Attention (T.O.V.A.) Version 9.0The Tova Company2017-05-17
K143468QbCheckQbtech AB2016-03-22
K133382QB TESTQbtech AB2014-03-24
K122149QBTESQbtech AB2012-10-17
K040894QBTESTQbtech AB2004-06-22
K020800OPTAX SYSTEMOptax Systems, Inc.2002-06-10
K911938DYNAVISION 2000Performance Ent.1991-08-02
K861304FAGAN TEST MACHINE FOR INFANT INTELLIGENCEInfantest Corp.1986-09-23
K854903GORDON DIAGNOSTIC SYSTEM MODEL IClinical Diagnostics, Inc.1986-06-02

Legacy Summary#

summary

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases