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QbTest

FDA UDI

Class U (US FDA UDI)

by Qbtech Inc

Identity

Trade Name
QbTest FDA UDI
Generic Name
Psychological assessment software FDA UDI
Model / Reference
QbTest FDA UDI

Identifiers

Primary DI / UDI-DI
07350103930067 FDA UDI
510(k) Number
K040894 FDA UDI
K122149 FDA UDI
K133382 FDA UDI
FDA Product Code
LQD FDA UDI
GMDN Term
Psychological assessment software FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Psychological assessment software

QbTest by Qbtech Inc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Psychological assessment software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qbtech Inc

Sources (1)

  • FDA UDI 9bdc8f0c-4bec-47a7-94d0-facaad89d5b9 33 fields · synced May 30, 2026