Product Code: LQD FDA unclassified

Recorder, Attention Task Performance

Unknown

The Attention Task Performance Recorder is a device used to measure and record a patient's performance on attention and cognitive tasks, typically used in neurological or psychological assessment to evaluate sustained attention, reaction time, or related cognitive functions. This device is currently unclassified (Class U) by the FDA, meaning it has not been placed into a final regulatory classification category. The product code is LQD; no regulation number or medical specialty is on file for this entry. No special flags apply to this device.

510(k)s
11
FEI Numbers
5
Registration Numbers
5
Unique Applicants
7
Years Active
32

Research product code LQD in seconds

The Research Assistant summarizes clearances, adverse event trends and regulation context for a product code — and cites every record.

Free to try · every answer cites its records

Basic Information

Product Code
LQD
Device Class
FDA unclassified
Medical Specialty
Unknown
Review Panel
NE
Submission Type
1

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

Unclassified Reason

1

510(k) Clearance History

Loading...

Related 510(k) Clearances

This FDA classification is associated with 11 510(k) clearances via K numbers.

K Number Device Name
K173915 Test of Variables of Attention (T.O.V.A.)
K170082 Test of Variables of Attention (T.O.V.A.) Version 9.0
K143468 QbCheck
K141865 DANA
K133382 QB TEST
K122149 QBTES
K040894 QBTEST
K020800 OPTAX SYSTEM
K911938 DYNAVISION 2000
K861304 FAGAN TEST MACHINE FOR INFANT INTELLIGENCE
K854903 GORDON DIAGNOSTIC SYSTEM MODEL I

FEI Numbers

This FDA classification entry is associated with 5 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 5 registration numbers. Click on an entry to view related FDA registrations.