510(k) Report

510(k) · Cleared

Cleared

Dell U3014 with Qubyx Perfectlum Bundle

K131601510(k) TraditionalCleared Jul 7, 2014399-day reviewClass II21 CFR 892.2050

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Qubyx Limited · PGY Display, Diagnostic Radiology

Cleared on Jul 7, 2014 as substantially equivalent to K111385 (Qubyx Limited, 2012) and 1 other predicate after a 399-day review. Its family tree reaches back 5 generations to 2004. 2 later devices descend from it.

Decided
Jul 7, 2014
Review
399 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K040982 (2004). 6 ancestors in all. 2 later devices descend from it, 1 citing it directly.

  1. Root · 5 generations backK040982 Color LCD Monitor, Model Radiforce R12Eizo Nanao Corporation · 2004
  2. 4 generations backK061305 Medical Display, MDC1900-1LG (1LR)Chi Lin Technology Co., Ltd. · 2006
  3. 3 generations backK063579 2MP Medical Color Reference Display, Model MDC2130-2HCChi Lin Technology Co., Ltd. · 2006
  4. 2 generations backK083916 LCD3090WQXI or MD304MC 29.8 Inch Diagnostic Imaging LCD Monitor…Nec Display Solutions, Ltd. · 2009
  5. 1 generation backK111237 MD301C4 29.8 Diagnostic Imaging LCD Monitor, L309TYNec Display Solutions, Ltd. · 2011
  6. This deviceK131601 Dell U3014 with Qubyx Perfectlum BundleQubyx Limited · 2014
  7. Descendant · cites it directly · 1 of its ownK171229 DELL UP3017 with QUBYX PerfectLum bundleQubyx Software Technologies, Inc. · 2017
  8. Descendant · 2 generations on · 0 of its ownK200889 iMac 27 & PL 4.0Quantum-Spectra, LLC · 2020

Most influential descendants

Showing 2 of 2 · See all
  • K171229DELL UP3017 with QUBYX PerfectLum bundleQubyx Software Technologies, Inc. · 2017 · cites it directly1descendant
  • K200889iMac 27 & PL 4.0Quantum-Spectra, LLC · 2020 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K040982Color LCD Monitor, Model Radiforce R12Eizo Nanao Corporation2004—
−4K061305Medical Display, MDC1900-1LG (1LR)Chi Lin Technology Co., Ltd.2006—
−3K0635792MP Medical Color Reference Display, Model MDC2130-2HCChi Lin Technology Co., Ltd.2006—
−2K083916LCD3090WQXI or MD304MC 29.8 Inch Diagnostic Imaging LCD Monitor, Model L307TDNec Display Solutions, Ltd.2009—
−1K111237MD301C4 29.8 Diagnostic Imaging LCD Monitor, L309TYNec Display Solutions, Ltd.2011—
0 (this device)K131601Dell U3014 with Qubyx Perfectlum BundleQubyx Limited2014—
+1K171229DELL UP3017 with QUBYX PerfectLum bundleQubyx Software Technologies, Inc.2017—
+2K200889iMac 27 & PL 4.0Quantum-Spectra, LLC2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
202010
FIG. 1 — Lineage of K131601, 2004–2020Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 PGY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new PGY device

  1. #1 K261213 Medical Monitor (40HT513D)score 13.9 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (2)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K111385Dell Ultrasharp U3011 W/Qubyx Perfectlum Bundle
Summary page 1
…6. Classification Number Medical displays classified in Class 11per 21 CFR 892.2050 7. Predicate device 1 Name: UltraShamp U3011 Manufacturer: DELL Inc. 510(k) number: K111385 Predicate device 2 Name: MD301 C4 Manufacturer: NEC Display Solutions Ltd. 51 0(k) number: K1 11237 8. Device description The…
Qubyx Limited2012—
*K111237MD301C4 29.8 Diagnostic Imaging LCD Monitor, L309TY
Summary page 1
…evice 1 Name: UltraShamp U3011 Manufacturer: DELL Inc. 510(k) number: K111385 Predicate device 2 Name: MD301 C4 Manufacturer: NEC Display Solutions Ltd. 51 0(k) number: K1 11237 8. Device description The DELL U3014 with QUBYX PerfectLum is a 30" color display for medical viewing. It provides 2560x1 600 r…
Nec Display Solutions, Ltd.2011—

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K171229DELL UP3017 with QUBYX PerfectLum bundleQubyx Software Technologies, Inc.20171

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 10 years and passes through 4 companies; a new generation was cleared every 2.1 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K171229 (Qubyx Software Technologies, Inc., 2017) has gone furthest, with 1 descendant of its own.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · PGY

3in 2025

2014: 142015: 162016: 182017: 112018: 52019: 112020: 122021: 72022: 102023: 172024: 102025: 32026 (partial year): 4
2007high 18 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PGY

59in 2025

2014: 24 days median2015: 31 days median2016: 27 days median2017: 30 days median2018: 28 days median2019: 58 days median2020: 61 days median2021: 77 days median2022: 60 days median2023: 60 days median2024: 53 days median2025: 59 days median2026 (partial year): 48 days median
2007high 77 (2021) · low 24 (2014)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · PGY

No recall names PGY since 2007.

Adverse event reports per year · PGY

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2025

MAUDE reports naming product code PGY, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
2014142400
2015163100
2016182700
2017113001
201852800
2019115800
2020126100
202177700
2022106000
2023176000
2024105300
202535900
20264480—

What is it indicated for?

The DELL U3014 with QUBYX PerfectLum is intended to be used for

displaying and viewing medical images, for review and analysis by trained

medical practitioners.

The DELL U3014 can be used only in conjunction with QUBYX

PerfectLum.

The device can not be used in primary image diagnosis in mammography.

The device can not be used for a life-support system.

The device does not contact with the patient.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131601: Dell U3014 with Qubyx Perfectlum Bundle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K131601

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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