510(k) Report

510(k) · Cleared

Cleared

JUSHA-C43 LCD Monitor

K151972510(k) TraditionalCleared Sep 10, 201556-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

Nanjing Jusha Display Technology Co., Ltd. · PGY Display, Diagnostic Radiology

Cleared on Sep 10, 2015 as substantially equivalent to K130070 (Eizo Nanao Corporation, 2013) after a 56-day review. Its family tree reaches back 1 generation to 2013.

Decided
Sep 10, 2015
Review
56 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K130070 (2013). No later device cites it as a predicate yet.

K130070 · 4MP Color LCD Monitor, Radiforce RX440 · Eizo Nanao Corporation · 20132010201220142016
  1. Root · 1 generation backK130070 4MP Color LCD Monitor, Radiforce RX440Eizo Nanao Corporation · 2013
  2. This deviceK151972 JUSHA-C43 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2015
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K1300704MP Color LCD Monitor, Radiforce RX440Eizo Nanao Corporation2013—
0 (this device)K151972JUSHA-C43 LCD MonitorNanjing Jusha Display Technology Co., Ltd.2015—
FIG. 1 — Lineage of K151972, 2013–2015Source: 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
*K1300704MP Color LCD Monitor, Radiforce RX440
Summary page 4
…4MP Color LCD Monitor Classification Name: System, image processing ,Radiology Product Code: PGY Predicate Device(s): RADIFORCE RX440;K130070 JUSHA-C43 LCD Monitoris the display system with the high Device Description:…
Eizo Nanao Corporation2013—

Also cleared against K130070: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K130070.

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?

JUSHA-C43 LCD Monitor is intended to be used in displaying and viewing digital images for review and analysis by trained medical practitioners. It does not support the display of mammography images for diagnosis.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151972: JUSHA-C43 LCD Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151972

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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