510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

RadiForce RX360, RX360-AR

K182591510(k) AbbreviatedCleared Oct 18, 201828-day reviewClass II21 CFR 892.2050Recalls 1

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

Eizo Corporation · PGY Display, Diagnostic Radiology

Cleared on Oct 18, 2018 as substantially equivalent to K153354 (Eizo Corporation, 2016) after a 28-day review. Its family tree reaches back 5 generations to 2004. 7 later devices descend from it. It has been recalled once.

Decided
Oct 18, 2018
Review
28 days
Class
Class II
Product code
PGY
Recalls
1
Predicates
1

Its longest line of descent runs back 5 generations to K033466 (2004). 7 later devices descend from it, 3 citing it directly.

  1. Root · 5 generations backK033466 Color LCD Display, Model Radiforce R22Eizo Nanao Corporation · 2004
  2. 4 generations backK052344 Color LCD Monitor, Model Radioforce R31 & R31-CEizo Nanao Corporation · 2005
  3. 3 generations backK090045 Color LCD Monitor, Radiforce RX320Eizo Nanao Corporation · 2009
  4. 2 generations backK113562 3MP Color LCD Monitor, Radiforce RX340Eizo Nanao Corporation · 2012
  5. 1 generation backK153354 3MP Color LCD Monitor, RadiForce RX350Eizo Corporation · 2016
  6. This deviceK182591 RadiForce RX360, RX360-AREizo Corporation · 2018
  7. Descendant · cites it directly · 4 of its ownK201211 3MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors…Shenzhen Beacon Display Technology Co., Ltd. · 2020
  8. Descendant · 2 generations on · 1 of its ownK240310 LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024
  9. Descendant · 3 generations on · 0 of its ownK243031 LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024
  10. Descendant · 2 generations on · 0 of its ownK233336 21.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp. · 2024
  11. Descendant · cites it directly · 0 of its ownK223768 RadiForce RX270Eizo Corporation · 2023

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2020: 12021: 12022: 12023: 12024: 3
2020high 3 (2024) · low 0 (2025)2026

Most influential descendants

Showing 5 of 7 · See all
  • K2012113MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+Shenzhen Beacon Display Technology Co., Ltd. · 2020 · cites it directly4descendants
  • K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024 · 2 generations on1descendant
  • K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024 · 3 generations on0descendants
  • K23333621.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp. · 2024 · 2 generations on0descendants
  • K223768RadiForce RX270Eizo Corporation · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K033466Color LCD Display, Model Radiforce R22Eizo Nanao Corporation2004—
−4K052344Color LCD Monitor, Model Radioforce R31 & R31-CEizo Nanao Corporation2005—
−3K090045Color LCD Monitor, Radiforce RX320Eizo Nanao Corporation2009—
−2K1135623MP Color LCD Monitor, Radiforce RX340Eizo Nanao Corporation2012—
−1K1533543MP Color LCD Monitor, RadiForce RX350Eizo Corporation2016—
0 (this device)K182591RadiForce RX360, RX360-AREizo Corporation2018—
+1K2012113MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+Shenzhen Beacon Display Technology Co., Ltd.2020—
+2K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024—
+3K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024—
+2K23333621.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp.2024—
+1K223768RadiForce RX270Eizo Corporation2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
202210
202310
202430
FIG. 1 — Lineage of K182591, 2004–2024Source: 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
*K1533543MP Color LCD Monitor, RadiForce RX350
Summary page 4
…(21 CFR 892.2050) • Regulatory Class: II • Product Code: PGY 3. Predicate Device EIZO Corporation RadiForce RX350 (K153354) Section 05 510(k) Summary_RX360: Page 1 of 4 4. Device De…
Eizo Corporation2016—

Also cleared against K153354: 4 other devices →

What descends from it? (7)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K2012113MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+Shenzhen Beacon Display Technology Co., Ltd.20204
K223768RadiForce RX270Eizo Corporation20230
K211491RadiForce RX370Eizo Corporation20210

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Jul 30, 2019Class IIZ-2294-2020Device DesignUnder certain conditions, a marble pattern infrequently appears on the monitor.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 14 years and passes through 2 companies; a new generation was cleared every 3.4 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K201211 (Shenzhen Beacon Display Technology Co., Ltd., 2020) has gone furthest, with 4 descendants of its own.
  • 4 other devices also cite its predicate K153354.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, 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?

This Product is indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182591: RadiForce RX360, RX360-AR.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K182591

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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