510(k) Report

510(k) · Cleared

Cleared

MD322C8 31.5 Diagnostic Imaging LCD Monitor

K150145510(k) TraditionalCleared Feb 6, 201515-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

Nec Display Solutions, Ltd. · PGY Display, Diagnostic Radiology

Cleared on Feb 6, 2015 as substantially equivalent to K142951 (Nec Display Solutions, Ltd., 2014) after a 15-day review. Its family tree reaches back 9 generations to 2000. 1 later device descends from it.

Decided
Feb 6, 2015
Review
15 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K000293 (2000). 1 later device descends from it, 1 citing it directly.

  1. Root · 9 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 5 generations between
  3. 3 generations backK090215 MD213MG 21.3 Diagnostic Imaging LCD Monitor - L218TLNec Display Solutions, Ltd. · 2009
  4. 2 generations backK130770 MD211C3 21.3 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd. · 2013
  5. 1 generation backK142951 MD210C3 21.3 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd. · 2014
  6. This deviceK150145 MD322C8 31.5 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd. · 2015
  7. Descendant · cites it directly · 0 of its ownK162196 Dell UP3216Q with QUBYX PerfectLum bundleQubyx Software Technologies, Inc. · 2016
Show all 9 generations
  1. Root · 9 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 8 generations backK012099 Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd. · 2001
  3. 7 generations backK022109 Eizo, Model FC-2091Eizo Nanao Corporation · 2002
  4. 6 generations backK041597 Monochrome LCD Monitor, Model Radiforce G22Eizo Nanao Corporation · 2004
  5. 5 generations backK061303 Medical Display, Models MDM 1900-1NG and MDM 1900-1NRChi Lin Technology Co., Ltd. · 2006
  6. 4 generations backK063266 3MP Medical Monochrome Reference Display, Model MDM2130-3NCChi Lin Technology Co., Ltd. · 2006
  7. 3 generations backK090215 MD213MG 21.3 Diagnostic Imaging LCD Monitor - L218TLNec Display Solutions, Ltd. · 2009
  8. 2 generations backK130770 MD211C3 21.3 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd. · 2013
  9. 1 generation backK142951 MD210C3 21.3 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd. · 2014
  10. This deviceK150145 MD322C8 31.5 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K162196Dell UP3216Q with QUBYX PerfectLum bundleQubyx Software Technologies, Inc. · 2016 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K000293Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V.2000—
−8K012099Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd.2001—
−7K022109Eizo, Model FC-2091Eizo Nanao Corporation2002—
−6K041597Monochrome LCD Monitor, Model Radiforce G22Eizo Nanao Corporation2004—
−5K061303Medical Display, Models MDM 1900-1NG and MDM 1900-1NRChi Lin Technology Co., Ltd.2006—
−4K0632663MP Medical Monochrome Reference Display, Model MDM2130-3NCChi Lin Technology Co., Ltd.2006—
−3K090215MD213MG 21.3 Diagnostic Imaging LCD Monitor - L218TLNec Display Solutions, Ltd.2009—
−2K130770MD211C3 21.3 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd.2013—
−1K142951MD210C3 21.3 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd.2014—
0 (this device)K150145MD322C8 31.5 Diagnostic Imaging LCD MonitorNec Display Solutions, Ltd.2015—
+1K162196Dell UP3216Q with QUBYX PerfectLum bundleQubyx Software Technologies, Inc.2016—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
FIG. 1 — Lineage of K150145, 2000–2016Source: 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K142951MD210C3 21.3 Diagnostic Imaging LCD Monitor
Summary page 4
…892.2050) Product Code: PGY 4. PREDICATE DEVICE MD210C3 3MP Color LCD Monitor by NEC Display Solutions Ltd. (K142951) 5. DEVICE DESCRIPTION Medical Display, MD322C8 is a 31.5” Color LCD monitor that displays image for medical use. I…
Nec Display Solutions, Ltd.2014—

Also cleared against K142951: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K162196Dell UP3216Q with QUBYX PerfectLum bundleQubyx Software Technologies, Inc.20160

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 15 years and passes through 5 companies; a new generation was cleared every 1.6 years on median.
  • None of the 9 ancestors has a recall.
  • Of its descendants, K162196 (Qubyx Software Technologies, Inc., 2016) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K142951.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, 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 MD322C8 color display is intended to be used for displaying and viewing of digital images for diagnosis by trained physicians.

To guarantee the display performance as specified, it must only be used for in Conjunction with NEC approved display controllers.

MD322C8 cannot be used for a life-support system.

This device must not be used in digital mammography.

This device is designed for exclusive interconnection with IEC60601-1-1 certified equipment.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K150145: MD322C8 31.5 Diagnostic Imaging LCD Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K150145

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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