510(k) Report

510(k) · Cleared

Cleared

3MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+

K201211510(k) TraditionalCleared Sep 3, 2020121-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

Shenzhen Beacon Display Technology Co., Ltd. · PGY Display, Diagnostic Radiology

Cleared on Sep 3, 2020 as substantially equivalent to K182591 (Eizo Corporation, 2018) and 1 other predicate after a 121-day review. Its family tree reaches back 7 generations to 2000. 4 later devices descend from it.

Decided
Sep 3, 2020
Review
121 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K000293 (2000). 13 ancestors in all. 4 later devices descend from it, 3 citing it directly.

Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor3 generations back: 1 other ancestor4 generations back: 1 other ancestor5 generations back: 1 other ancestor6 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 1 descendant K113784 · 3MP Monochrome LCD Monitor, Radiforce GX340 · Eizo Nanao Corporation · 2012K062053 · Monochrome LCD Monitor, Radiforce, GS320 · Eizo Nanao Corporation · 2006K060845 · Monochrome LCD Monitor, Radiforce Model GS310 · Eizo Nanao Corporation · 2006K052337 · Monochrome LCD Monitor, Model Radiforce G33 · Eizo Nanao Corporation · 2005K022109 · Eizo, Model FC-2091 · Eizo Nanao Corporation · 2002K012099 · Monochrome Perfectly Flat Panel Displays, ME Series · Totoku Electric Co., Ltd. · 2001K000293 · Barco MGD 221 2 Megapixel Diagnostic Display · Barco N.V. · 2000−50
  1. Root · 7 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 6 generations backK012099 Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd. · 2001
  3. 5 generations backK022109 Eizo, Model FC-2091Eizo Nanao Corporation · 2002
  4. 4 generations backK052337 Monochrome LCD Monitor, Model Radiforce G33Eizo Nanao Corporation · 2005
  5. 3 generations backK060845 Monochrome LCD Monitor, Radiforce Model GS310Eizo Nanao Corporation · 2006
  6. 2 generations backK062053 Monochrome LCD Monitor, Radiforce, GS320Eizo Nanao Corporation · 2006
  7. 1 generation backK113784 3MP Monochrome LCD Monitor, Radiforce GX340Eizo Nanao Corporation · 2012
  8. This deviceK201211 3MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors…Shenzhen Beacon Display Technology Co., Ltd. · 2020
  9. Descendant · cites it directly · 1 of its ownK240310 LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024
  10. Descendant · 2 generations on · 0 of its ownK243031 LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024
  11. Descendant · cites it directly · 0 of its ownK233336 21.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp. · 2024
  12. Descendant · cites it directly · 0 of its ownK221567 LCD monitor (HMD3C21S), LCD monitor (HMD5G21S)Qingdao Hisense Medical Equipment Co., Ltd. · 2022

Most influential descendants

Showing 4 of 4 · See all
  • K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024 · cites it directly1descendant
  • K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd. · 2024 · 2 generations on0descendants
  • K23333621.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp. · 2024 · cites it directly0descendants
  • K221567LCD monitor (HMD3C21S), LCD monitor (HMD5G21S)Qingdao Hisense Medical Equipment Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K000293Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V.2000—
−6K012099Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd.2001—
−5K022109Eizo, Model FC-2091Eizo Nanao Corporation2002—
−4K052337Monochrome LCD Monitor, Model Radiforce G33Eizo Nanao Corporation2005—
−3K060845Monochrome LCD Monitor, Radiforce Model GS310Eizo Nanao Corporation2006—
−2K062053Monochrome LCD Monitor, Radiforce, GS320Eizo Nanao Corporation2006—
−1K1137843MP Monochrome LCD Monitor, Radiforce GX340Eizo Nanao Corporation2012—
0 (this device)K2012113MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+Shenzhen Beacon Display Technology Co., Ltd.2020—
+1K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024—
+2K243031LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.2024—
+1K23333621.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp.2024—
+1K221567LCD monitor (HMD3C21S), LCD monitor (HMD5G21S)Qingdao Hisense Medical Equipment Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200410
200510
200910
201210
201610
201810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202430
FIG. 1 — Lineage of K201211, 2000–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
Get a 510(k) Report

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
*K182591RadiForce RX360, RX360-AR
Summary page 5
…C32S+, C32SP+, G32S+, G32SP+ 510(k) Submission EIZO Corporation, RadiForce RX360, RX360-AR has been cleared by FDA through 510(k) No. K182591 (Decision Date - October 18, 2018). EIZO NANAO Corporation, 3MP Monochrome LCD Monitor, RadiForce GX340 has been cleared by…
Eizo Corporation20181
*K1137843MP Monochrome LCD Monitor, Radiforce GX340
Summary page 5
…k) No. K182591 (Decision Date - October 18, 2018). EIZO NANAO Corporation, 3MP Monochrome LCD Monitor, RadiForce GX340 has been cleared by FDA through 510(k) No. K113784 (Decision Date - May 4, 2012). 5. Description of the Device [21 CFR 807.92(a) (4)] 3MP Color LCD monitors C32S+, C32SP+; 3MP…
Eizo Nanao Corporation2012—

Also cleared against K182591: 2 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K240310LCD Monitors C310S, G310S, C316S, G316S, C616WShenzhen Beacon Display Technology Co., Ltd.20241
K23333621.3” 3MP Color LCD Display UMD3-21B01 (MD3-21B01)Acula Technology Corp.20240
K221567LCD monitor (HMD3C21S), LCD monitor (HMD5G21S)Qingdao Hisense Medical Equipment Co., Ltd.20220

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 20 years and passes through 4 companies; a new generation was cleared every 1.3 years on median.
  • 1 of the 13 ancestors has a recall of any class.
  • Of its descendants, K240310 (Shenzhen Beacon Display Technology Co., Ltd., 2024) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K182591.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, 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 3MP Color LCD Monitors C32S+, C32SP+ are indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The displays are not intended for mammography.

The 3MP Monochrome LCD Monitors G32S+, G32SP+ are intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The devices are not specified for digital mammography systems.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201211: 3MP Color LCD Monitors C32S+, C32SP+; 3MP Monochrome LCD Monitors G32S+, G32SP+.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K201211

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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