LQD — Recorder, Attention Task Performance Class U

FDA Device Classification

FDA product code LQD covers "Recorder, Attention Task Performance", a Class U medical device. Submissions are reviewed by the Unknown panel. At least 11 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LQD
Device Class
Class U
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K173915tovaTest of Variables of Attention (T.O.V.A.)March 22, 2018
K170082tovaTest of Variables of Attention (T.O.V.A.) Version 9.0May 17, 2017
K143468qbtechQbCheckMarch 22, 2016
K141865anthrotronixDANAOctober 15, 2014
K133382qbtechQB TESTMarch 24, 2014
K122149qbtechQBTESOctober 17, 2012
K040894qbtechQBTESTJune 22, 2004
K020800optax systemsOPTAX SYSTEMJune 10, 2002
K911938performance entDYNAVISION 2000August 2, 1991
K861304infantestFAGAN TEST MACHINE FOR INFANT INTELLIGENCESeptember 23, 1986
K854903clinical diagnosticsGORDON DIAGNOSTIC SYSTEM MODEL IJune 2, 1986