510(k) · Cleared
ClearedQBTES
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Qbtech AB · LQD Recorder, Attention Task Performance
Cleared on Oct 17, 2012 as substantially equivalent to K040894 (Qbtech AB, 2004) after a 90-day review. Its family tree reaches back 3 generations to 1986. 4 later devices descend from it.
- Decided
- Oct 17, 2012
- Review
- 90 days
- Class
- Class U
- Product code
- LQD
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K854903 (1986). 4 later devices descend from it, 2 citing it directly.
- Root · 3 generations backK854903 Gordon Diagnostic System Model IClinical Diagnostics, Inc. · 1986
- 2 generations backK020800 Optax SystemOptax Systems, Inc. · 2002
- 1 generation backK040894 QbtestQbtech AB · 2004
- This deviceK122149 QBTESQbtech AB · 2012
- Descendant · cites it directly · 2 of its ownK133382 QB TestQbtech AB · 2014
- Descendant · 2 generations on · 0 of its ownK173915 Test of Variables of Attention (T.O.V.A.)The Tova Company · 2018
- Descendant · 2 generations on · 0 of its ownK143468 QbCheckQbtech AB · 2016
- Descendant · cites it directly · 0 of its ownK141865 DANAAnthrotronix, Inc. · 2014
Most influential descendants
Showing 4 of 4 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K854903 | Gordon Diagnostic System Model I | Clinical Diagnostics, Inc. | 1986 | — |
| −2 | K020800 | Optax System | Optax Systems, Inc. | 2002 | — |
| −1 | K040894 | Qbtest | Qbtech AB | 2004 | — |
| 0 (this device) | K122149 | QBTES | Qbtech AB | 2012 | — |
| +1 | K133382 | QB Test | Qbtech AB | 2014 | — |
| +2 | K173915 | Test of Variables of Attention (T.O.V.A.) | The Tova Company | 2018 | — |
| +2 | K143468 | QbCheck | Qbtech AB | 2016 | — |
| +1 | K141865 | DANA | Anthrotronix, Inc. | 2014 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 2 | 0 |
| 2016 | 1 | 0 |
| 2018 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in LQD? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K040894 | QbtestSummary page 1…ans.bostrom~qbtech.se Trade Name: QbTest Classification name: Recorder, attention task performance Product Code: LQD Predicate Device: QbTest (K040894) and Gordon Diagnostic System (K854903) Descripti Gordon [QbTest (K040894)… | 2004 |
| † | K854903 | Gordon Diagnostic System Model I | 1986 |
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 26 years and passes through 3 companies; a new generation was cleared every 8.3 years on median.
- None of the 3 ancestors has a recall.
- Of its descendants, K133382 (Qbtech AB, 2014) has gone furthest, with 2 descendants of its own.
How does its category compare?
All LQD devicesLQD Recorder, Attention Task Performance: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · LQD
1in 2018
2026 to Oct 25, outlined.
Median 510(k) review, days · LQD
Too few LQD 510(k)s in any year since 2007 to give a median.
Recalls per year · LQD
No recall names LQD since 2007.
Adverse event reports per year · LQD
No MAUDE report names LQD since 2007.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 2 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
QbTest provides clinicians with objective measurements of hyperactivity, impulsivity, and
inattention to aid in the clinical assessment of ADHD. QbTest results should be interpreted only
by qualified professionals.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K122149 · printed Nov 6, 2026
Cite this page
510(k) Report. “K122149: QBTES.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122149
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026