FDA product code QFT

Digital Therapeutic Software For Attention Deficit Hyperactivity Disorder

Obstetrics/Gynecology·Class 2·21 CFR 882.5803
US regulatory classifications
US Product Code (FDA)
QFT
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US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 882.5803
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Medical specialty
Obstetrics/Gynecology
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
Definition

A digital therapy device for Attention Deficit Hyperactivity Disorder (ADHD) is a software intended to provide therapy for ADHD or any of its individual symptoms as an adjunct to clinician supervised treatment.

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About this record

Digital Therapeutic Software For Attention Deficit Hyperactivity Disorder is a medical device type in the Obstetrics/Gynecology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.