510(k) Report

510(k) · Cleared

Cleared

Barco 5MP Mammo, Model MDMG-5221

K090603510(k) TraditionalCleared Apr 22, 200948-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

Barco N.V. · LLZ System, Image Processing, Radiological

Cleared on Apr 22, 2009 after a 48-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 5 later devices descend from it.

Decided
Apr 22, 2009
Review
48 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
0

5 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2016: 1 descendant cleared2019: 1 descendant cleared2023: 2 descendants cleared2022: 1 descendant cleared20052010201520202025
  1. This deviceK090603 Barco 5MP Mammo, Model MDMG-5221Barco N.V. · 2009
  2. Descendant · cites it directly · 4 of its ownK161229 Mammo Tomosynthesis (MDMG-5221)Barco N.V. · 2016
  3. Descendant · 2 generations on · 2 of its ownK190848 JUSHA-M550G/ JUSHA-M550/M550G/M550 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2019
  4. Descendant · 2 generations on · 0 of its ownK231170 C350/C350G LCD Monitor; M550/M550G LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2023
  5. Descendant · 3 generations on · 0 of its ownK230723 C510G/JUSHA-C510G/C510/JUSHA- C510 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2023
  6. Descendant · 3 generations on · 0 of its ownK212231 C1210G LCD Monitor, JUSHA-C1210G LCD Monitor, C1210 LCD Monitor…Nanjing Jusha Display Technology Co., Ltd. · 2022

Most influential descendants

Showing 5 of 5 · See all
  • K161229Mammo Tomosynthesis (MDMG-5221)Barco N.V. · 2016 · cites it directly4descendants
  • K190848JUSHA-M550G/ JUSHA-M550/M550G/M550 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2019 · 2 generations on2descendants
  • K231170C350/C350G LCD Monitor; M550/M550G LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2023 · 2 generations on0descendants
  • K230723C510G/JUSHA-C510G/C510/JUSHA- C510 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2023 · 3 generations on0descendants
  • K212231C1210G LCD Monitor, JUSHA-C1210G LCD Monitor, C1210 LCD Monitor, JUSHA-C1210 LCD MonitorNanjing Jusha Display Technology Co., Ltd. · 2022 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K090603Barco 5MP Mammo, Model MDMG-5221Barco N.V.2009—
+1K161229Mammo Tomosynthesis (MDMG-5221)Barco N.V.2016—
+2K190848JUSHA-M550G/ JUSHA-M550/M550G/M550 LCD MonitorNanjing Jusha Display Technology Co., Ltd.2019—
+2K231170C350/C350G LCD Monitor; M550/M550G LCD MonitorNanjing Jusha Display Technology Co., Ltd.2023—
+3K230723C510G/JUSHA-C510G/C510/JUSHA- C510 LCD MonitorNanjing Jusha Display Technology Co., Ltd.2023—
+3K212231C1210G LCD Monitor, JUSHA-C1210G LCD Monitor, C1210 LCD Monitor, JUSHA-C1210…Nanjing Jusha Display Technology Co., Ltd.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201910
202210
202320
FIG. 1 — Lineage of K090603, 2009–2023Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LLZ? 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 LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (5)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K161229Mammo Tomosynthesis (MDMG-5221)Barco N.V.20164

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?

  • Of its descendants, K161229 (Barco N.V., 2016) has gone furthest, with 4 descendants of its own.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

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

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

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

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, 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
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

The Barco 5MP Mammo device is intended to be used in displaying and viewing digital images, including standard and multi-frame digital mammography, for review and analysis by trained medical practitioners.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K090603: Barco 5MP Mammo, Model MDMG-5221.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K090603

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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