510(k) Report

510(k) · Cleared

Cleared

Hisense LCD monitor HMD2G21S, HMD3G21S

K222132510(k) TraditionalCleared Nov 8, 2022112-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

Qingdao Hisense Medical Equipment Co., Ltd. · PGY Display, Diagnostic Radiology

Cleared on Nov 8, 2022 as substantially equivalent to K183497 (Nanjing Jusha Display Technology Co., Ltd., 2019) and 1 other predicate after a 112-day review. Its family tree reaches back 8 generations to 2000.

Decided
Nov 8, 2022
Review
112 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K000293 (2000). 9 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK000293 Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V. · 2000
  2. 7 generations backK012099 Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd. · 2001
  3. 6 generations backK022109 Eizo, Model FC-2091Eizo Nanao Corporation · 2002
  4. 5 generations backK052337 Monochrome LCD Monitor, Model Radiforce G33Eizo Nanao Corporation · 2005
  5. 4 generations backK060845 Monochrome LCD Monitor, Radiforce Model GS310Eizo Nanao Corporation · 2006
  6. 3 generations backK062053 Monochrome LCD Monitor, Radiforce, GS320Eizo Nanao Corporation · 2006
  7. 2 generations backK113784 3MP Monochrome LCD Monitor, Radiforce GX340Eizo Nanao Corporation · 2012
  8. 1 generation backK141690 Jusha-M33C LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2014
  9. This deviceK222132 Hisense LCD monitor HMD2G21S, HMD3G21SQingdao Hisense Medical Equipment Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K000293Barco MGD 221 2 Megapixel Diagnostic DisplayBarco N.V.2000—
−7K012099Monochrome Perfectly Flat Panel Displays, ME SeriesTotoku Electric Co., Ltd.2001—
−6K022109Eizo, Model FC-2091Eizo Nanao Corporation2002—
−5K052337Monochrome LCD Monitor, Model Radiforce G33Eizo Nanao Corporation2005—
−4K060845Monochrome LCD Monitor, Radiforce Model GS310Eizo Nanao Corporation2006—
−3K062053Monochrome LCD Monitor, Radiforce, GS320Eizo Nanao Corporation2006—
−2K1137843MP Monochrome LCD Monitor, Radiforce GX340Eizo Nanao Corporation2012—
−1K141690Jusha-M33C LCD MonitorNanjing Jusha Display Technology Co., Ltd.2014—
0 (this device)K222132Hisense LCD monitor HMD2G21S, HMD3G21SQingdao Hisense Medical Equipment Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201910
FIG. 1 — Lineage of K222132, 2000–2022Source: 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? (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
*K183497JUSHA-M260G LCD Monitor, JUSHA-M260 LCD Monitor, M260G LCD Monitor, M260 LCD Monitor
Summary page 5
…ology 21CFR 892.2050 Product Code: PGY 3. Predicate Device(s): Trade Name JUSHA-M260G LCD Monitor 510(k) Number K183497 Product Code PGY Manufacturer Nanjing Jusha Display Technology Co., Ltd Trade Name…
Nanjing Jusha Display Technology Co., Ltd.2019—
*K141690Jusha-M33C LCD Monitor
Summary page 5
…PGY Manufacturer Nanjing Jusha Display Technology Co., Ltd Trade Name JUSHA-M33C LCD Monitor 510(k) Number K141690 Product Code PGY Manufacturer Nanjing Jusha Display Technology Co., Ltd…
Nanjing Jusha Display Technology Co., Ltd.2014—

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?

  • The line of descent spans 22 years and passes through 5 companies; a new generation was cleared every 2.4 years on median.
  • None of the 9 ancestors has a recall.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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?

1) The 2MP Monochrome LCD Monitor HMD2G21S is intended to be used in displaying and viewing digital images for

diagnosis of X-ray or MRI, etc. by trained medical practitioners.

The device does not support the display of mammography images for diagnosis.

2)The 3MP Monochrome LCD Monitor HMD3G21S is intended to be used in displaying and viewing digital images for

diagnosis X-ray or MRI, etc. by trained medical practitioners.

The device does not support the display of mammography images for diagnosis.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K222132: Hisense LCD monitor HMD2G21S, HMD3G21S.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222132

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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