510(k) Report

510(k) · Cleared

Cleared

20.1 inch (51cm) Monochrome LCD Monitor ME205 (ML20205)

K143076510(k) TraditionalCleared Nov 12, 201416-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

Jvckenwood Corporation · PGY Display, Diagnostic Radiology

Cleared on Nov 12, 2014 as substantially equivalent to K021738 (Totoku Electric Co., Ltd., 2002) after a 16-day review. Its family tree reaches back 3 generations to 2000. 1 later device descends from it.

Decided
Nov 12, 2014
Review
16 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K000293 (2000). 1 later device descends from it, 1 citing it directly.

  1. Root · 3 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 2 generations backK012099 Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd. · 2001
  3. 1 generation backK021738 Flat Panel Displays, ME Series & CCL SeriesTotoku Electric Co., Ltd. · 2002
  4. This deviceK143076 20.1 inch (51cm) Monochrome LCD Monitor ME205 (ML20205)Jvckenwood Corporation · 2014
  5. Descendant · cites it directly · 0 of its ownK170944 LCD Monitor (MD310C, MD310G, MD210G)Benq Corporation · 2017

Most influential descendants

Showing 1 of 1 · See all
  • K170944LCD Monitor (MD310C, MD310G, MD210G)Benq Corporation · 2017 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K000293Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V.2000—
−2K012099Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd.2001—
−1K021738Flat Panel Displays, ME Series & CCL SeriesTotoku Electric Co., Ltd.2002—
0 (this device)K14307620.1 inch (51cm) Monochrome LCD Monitor ME205 (ML20205)Jvckenwood Corporation2014—
+1K170944LCD Monitor (MD310C, MD310G, MD210G)Benq Corporation2017—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
FIG. 1 — Lineage of K143076, 2000–2017Source: 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
*K021738Flat Panel Displays, ME Series & CCL Series
Summary page 4
…0 Picture Archiving and Communication System) Predicate Device: 20.1 inch (51 cm) Monochrome LCD Monitor ME201 (MDL2006A) (K021738) Device Description: ME205 (ML20205) is a 20.1-inch (51 cm) Monochrome LCD monitor w…
Totoku Electric Co., Ltd.2002—

Also cleared against K021738: 5 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K170944LCD Monitor (MD310C, MD310G, MD210G)Benq Corporation20170

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 14 years and passes through 3 companies; a new generation was cleared every 1.3 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K170944 (Benq Corporation, 2017) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K021738.

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?

20.1 inch (51 cm) Monochrome 2M pixel LCD Monitor ME205 (ML20205) is intended to be used in displaying and viewing medical images for diagnosis by trained Medical practitioners. It is not meant to be used in digital mammography.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K143076: 20.1 inch (51cm) Monochrome LCD Monitor ME205 (ML20205).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K143076

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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