510(k) · Cleared
ClearedLCD Monitor (CL1902A, CL2103F)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Shenzhen Beacon Display Technology Co., Ltd. · PGY Display, Diagnostic Radiology
Cleared on Dec 19, 2025 as substantially equivalent to K230684 (Eizo Corporation, 2023) and 1 other predicate after a 108-day review. Its family tree reaches back 4 generations to 2010.
- Decided
- Dec 19, 2025
- Review
- 108 days
- Class
- Class II
- Product code
- PGY
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 4 generations to K092613 (2010). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 4 generations backK092613 Color LCD Monitor, Model Radiforce RS210Eizo Nanao Corporation · 2010
- 3 generations backK131090 2MP Color LCD Monitor, Radiforce MX215Eizo Corporation · 2013
- 2 generations backK190153 RadiForce MX216Eizo Corporation · 2019
- 1 generation backK230684 RadiForce MX217Eizo Corporation · 2023
- This deviceK252780 LCD Monitor (CL1902A, CL2103F)Shenzhen Beacon Display Technology Co., Ltd. · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K092613 | Color LCD Monitor, Model Radiforce RS210 | Eizo Nanao Corporation | 2010 | — |
| −3 | K131090 | 2MP Color LCD Monitor, Radiforce MX215 | Eizo Corporation | 2013 | — |
| −2 | K190153 | RadiForce MX216 | Eizo Corporation | 2019 | — |
| −1 | K230684 | RadiForce MX217 | Eizo Corporation | 2023 | — |
| 0 (this device) | K252780 | LCD Monitor (CL1902A, CL2103F) | Shenzhen Beacon Display Technology Co., Ltd. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
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 K261213 Medical Monitor (40HT513D)score 13.9 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K230684 | RadiForce MX217Summary page 5…lass: II 3. Identification of Predicate Device(s) The identified predicate within this submission is as follows: EIZO Corporation, RadiForce MX217, K230684; EIZO Corporation, RadiForce MX194, K180961. 4. Description of the Device 1.3MP LCD Monitor CL1902A is a 19-inch TFT L… | 2023 |
| * | K180961 | RadiForce MX194Summary page 5…cate Device(s) The identified predicate within this submission is as follows: EIZO Corporation, RadiForce MX217, K230684; EIZO Corporation, RadiForce MX194, K180961. 4. Description of the Device 1.3MP LCD Monitor CL1902A is a 19-inch TFT LCD monitor, which is specifically designed to pr… | 2018 |
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 15 years and passes through 3 companies; a new generation was cleared every 4.2 years on median.
- None of the 5 ancestors has a recall.
How does its category compare?
All PGY devicesPGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · PGY
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · PGY
59in 2025
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
MAUDE reports naming product code PGY, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 14 | 24 | 0 | 0 |
| 2015 | 16 | 31 | 0 | 0 |
| 2016 | 18 | 27 | 0 | 0 |
| 2017 | 11 | 30 | 0 | 1 |
| 2018 | 5 | 28 | 0 | 0 |
| 2019 | 11 | 58 | 0 | 0 |
| 2020 | 12 | 61 | 0 | 0 |
| 2021 | 7 | 77 | 0 | 0 |
| 2022 | 10 | 60 | 0 | 0 |
| 2023 | 17 | 60 | 0 | 0 |
| 2024 | 10 | 53 | 0 | 0 |
| 2025 | 3 | 59 | 0 | 0 |
| 2026 | 4 | 48 | 0 | — |
What is it indicated for?
CL1902A and CL2103F are 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.
https://510kreport.com/device/K252780 · printed Nov 5, 2026
Cite this page
510(k) Report. “K252780: LCD Monitor (CL1902A, CL2103F).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K252780
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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