510(k) Report

510(k) · Cleared

Cleared

LLX240AB01

K102587510(k) TraditionalCleared Dec 1, 201083-day reviewClass II21 CFR 892.1680

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

Samsung Mobile Display Co., Ltd. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Dec 1, 2010 as substantially equivalent to K031447 (Canon, Inc., 2003) after an 83-day review. Its family tree reaches back 4 generations to 1998. 37 later devices descend from it.

Decided
Dec 1, 2010
Review
83 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K981556 (1998). 5 ancestors in all. 37 later devices descend from it, 7 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2011: 1 descendant cleared2021: 4 descendants cleared2015: 3 descendants cleared2012: 1 descendant cleared2016: 3 descendants cleared2017: 5 descendants cleared2018: 6 descendants cleared2020: 4 descendants cleared2019: 1 descendant cleared2022: 2 descendants cleared2024: 4 descendants cleared2023: 1 descendant cleared2025: 1 descendant cleared2026: 1 descendant clearedK981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 1998K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 20031995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 7 descendants2 generations forward: 6 descendants3 generations forward: 10 descendants4 generations forward: 4 descendants5 generations forward: 3 descendants6 generations forward: 4 descendants7 generations forward: 3 descendants K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 2003K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 19980+5
  1. Root · 4 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 3 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 2 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 1 generation backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. This deviceK102587 LLX240AB01Samsung Mobile Display Co., Ltd. · 2010
  6. Descendant · cites it directly · 20 of its ownK153401 GR40CWSamsung Electronics Co., Ltd. · 2015
  7. Descendant · 2 generations on · 18 of its ownK180543 GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85Samsung Electronics Co., Ltd. · 2018
  8. Descendant · 3 generations on · 10 of its ownK181626 Digital Diagnostic Mobile X-ray SystemSamsung Electronics Co., Ltd. · 2018
  9. Descendant · cites it directly · 8 of its ownK150150 1717SGN / 1717SCN Digital Flat Panel X-ray DetectorRayence Co., Ltd. · 2015
  10. Descendant · 3 generations on · 5 of its ownK181631 GR40CWSamsung Electronics Co., Ltd. · 2018

Showing 5 of 37 descendants. See all descendants

Descendants cleared per year

2011: 12012: 12015: 32016: 32017: 52018: 62019: 12020: 42021: 42022: 22023: 12024: 42025: 12026: 1
2011high 6 (2018) · low 0 (2013)2026

Most influential descendants

Showing 5 of 37 · See all
  • K153401GR40CWSamsung Electronics Co., Ltd. · 2015 · cites it directly20descendants
  • K180543GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85Samsung Electronics Co., Ltd. · 2018 · 2 generations on18descendants
  • K181626Digital Diagnostic Mobile X-ray SystemSamsung Electronics Co., Ltd. · 2018 · 3 generations on10descendants
  • K1501501717SGN / 1717SCN Digital Flat Panel X-ray DetectorRayence Co., Ltd. · 2015 · cites it directly8descendants
  • K181631GR40CWSamsung Electronics Co., Ltd. · 2018 · 3 generations on5descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−3K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−2K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−1K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
0 (this device)K102587LLX240AB01Samsung Mobile Display Co., Ltd.2010—
+1K153401GR40CWSamsung Electronics Co., Ltd.2015—
+2K180543GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85Samsung Electronics Co., Ltd.2018—
+3K181626Digital Diagnostic Mobile X-ray SystemSamsung Electronics Co., Ltd.2018—
+1K1501501717SGN / 1717SCN Digital Flat Panel X-ray DetectorRayence Co., Ltd.2015—
+3K181631GR40CWSamsung Electronics Co., Ltd.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201210
201530
201630
201750
201860
201910
202040
202140
202220
202310
202440
202510
202610
FIG. 1 — Lineage of K102587, 1998–2026Source: 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 MQB? 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 MQB device

  1. #1 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 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? (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
*K031447Canon, Digital Radiography, Model Cxdi-50G
Summary page 1
…al Flat Panel X-Ray Detector Classification Name : Solid State X-ray Imaging Device 3. Predicate Device : Manufacturer : Canon Inc. Device . : CXDI-50G 510(k) Number : K031447 (Decision Date - Mar. 26. 2003) - 4. Classifications Names & Citations : 21CFR 892.1650, MQB, Solid State X-ray Imaging Device,…
Canon, Inc.2003—

Also cleared against K031447: 15 other devices →

What descends from it? (37)

See all 37

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

NumberDeviceApplicantDecidedDescendants
K153401GR40CWSamsung Electronics Co., Ltd.201520
K1501501717SGN / 1717SCN Digital Flat Panel X-ray DetectorRayence Co., Ltd.20158
K160204BSD4343 Digital Flat Panel X-ray DetectorBontech, Inc.20162
K212051Rfa-1717DIG, Rfa-1717DICAstel, Inc.20210
K151014Aura DR 43C-AG flat panel detectorAbyzr Co., Ltd.20150
K102327Clearvision DR 7000FJpi Healthcare Co, Ltd.20120
K112558Digital Flat Panel X-Ray DetectorSamsung Mobile Display Co., Ltd.20110

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 12 years and passes through 3 companies; a new generation was cleared every 3.1 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K153401 (Samsung Electronics Co., Ltd., 2015) has gone furthest, with 20 descendants of its own.
  • 15 other devices also cite its predicate K031447.

How does its category compare?

All MQB devices

MQB Solid State X-Ray Imager (Flat Panel/Digital Imager): FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · MQB

8in 2025

2007: 132008: 82009: 152010: 112011: 242012: 222013: 212014: 322015: 212016: 222017: 312018: 162019: 222020: 192021: 212022: 312023: 102024: 82025: 82026 (partial year): 3
2007high 32 (2014) · low 8 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQB

127in 2025

2007: 22 days median2008: 15 days median2009: 57 days median2010: 116 days median2011: 102 days median2012: 80 days median2013: 105 days median2014: 102 days median2015: 81 days median2016: 92 days median2017: 30 days median2018: 30 days median2019: 30 days median2020: 28 days median2021: 48 days median2022: 48 days median2023: 30 days median2024: 187 days median2025: 127 days median2026 (partial year): 245 days median
2007high 245 (2026) · low 15 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MQB

1in 2025

2007: 152008: 362009: 192010: 142011: 102012: 82013: 62017: 12018: 42019: 12020: 42021: 12025: 12026 (partial year): 1
2007high 36 (2008) · low 0 (2014)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MQB

141in 2025

2007: 252008: 302009: 342010: 392011: 1012012: 2672013: 1592014: 292015: 212016: 262017: 202018: 842019: 452020: 92021: 262022: 132023: 512024: 912025: 141
2007high 267 (2012) · low 9 (2020)2025

MAUDE reports naming product code MQB, 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
200713221525
20088153630
200915571934
2010111161439
20112410210101
201222808267
2013211056159
201432102029
20152181021
20162292026
20173130120
20181630484
20192230145
2020192849
20212148126
20223148013
20231030051
20248187091
202581271141
202632451—

What is it indicated for?

LLX240ABO! digital flat panel X-Ray detector is indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy targeting both adult and children. It is intended to replace-film based radiographic diagnostic systems and provide a case dfagnosis and treatment planning for physicians and other health care professionals. Not to be used for mammography.

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. “K102587: LLX240AB01.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102587

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