510(k) · Cleared
ClearedNio 5MP-21 and MDNG-5121 CB
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Barcoview · LLZ System, Image Processing, Radiological
Cleared on Mar 19, 2007 as substantially equivalent to K042221 (Barco NV Barcoview, 2004) after a 195-day review. Its family tree reaches back 6 generations to 2000. 1 later device descends from it.
- Decided
- Mar 19, 2007
- Review
- 195 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K001753 (2000). 7 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 6 generations backK001753 Medis 5MP2 Dual-Head Medical Diagnostic Display SystemBarco NV Display Systems · 2000
- 5 generations backK013922 Coronis 3MP Medicl Flat Panel Display SystemBarco N.V. · 2002
- 4 generations backK023341 Cornis 5MP Medical Flat Panel Display SystemBarco N.V. · 2002
- 3 generations backK032202 Dome CX Digital Flat-Panel Display System, Models C2 and C5IPlanar Systems, Inc. · 2003
- 2 generations backK040443 Dome CX Digital Flat-Panel Display System, Model C5IDome Imaging Systems, Inc. · 2004
- 1 generation backK042221 Coronis 5MP Medical Flat Panel Display SystemBarco NV Barcoview · 2004
- This deviceK062621 Nio 5MP-21 and MDNG-5121 CBBarcoview · 2007
- Descendant · cites it directly · 0 of its ownK132610 5MP Grayscale LCD DisplayShenzhen Beacon Display Technology Co., Ltd. · 2013
Most influential descendants
Showing 1 of 1 · See all- K1326105MP Grayscale LCD DisplayShenzhen Beacon Display Technology Co., Ltd. · 2013 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K001753 | Medis 5MP2 Dual-Head Medical Diagnostic Display System | Barco NV Display Systems | 2000 | — |
| −5 | K013922 | Coronis 3MP Medicl Flat Panel Display System | Barco N.V. | 2002 | — |
| −4 | K023341 | Cornis 5MP Medical Flat Panel Display System | Barco N.V. | 2002 | — |
| −3 | K032202 | Dome CX Digital Flat-Panel Display System, Models C2 and C5I | Planar Systems, Inc. | 2003 | — |
| −2 | K040443 | Dome CX Digital Flat-Panel Display System, Model C5I | Dome Imaging Systems, Inc. | 2004 | — |
| −1 | K042221 | Coronis 5MP Medical Flat Panel Display System | Barco NV Barcoview | 2004 | — |
| 0 (this device) | K062621 | Nio 5MP-21 and MDNG-5121 CB | Barcoview | 2007 | — |
| +1 | K132610 | 5MP Grayscale LCD Display | Shenzhen Beacon Display Technology Co., Ltd. | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 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 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 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K042221 | Coronis 5MP Medical Flat Panel Display SystemSummary page 1…ication name: System, Image Processing * Classification number: 21 CFR 892.2050 / Procode 9OLLZ 5. Predicate device * Name: Coronis SMP * 510(k) number: K042221 * Manufacturer: Barco NV 6. Device description Nio 5MP-21" is a display system for medical viewing. It consists of 3 comp… | 2004 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K132610 | 5MP Grayscale LCD Display | 2013 | 0 |
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 7 years and passes through 6 companies; a new generation was cleared every 11 months on median.
- None of the 7 ancestors has a recall.
- Of its descendants, K132610 (Shenzhen Beacon Display Technology Co., Ltd., 2013) has gone furthest, with 0 descendants of its own.
- 3 other devices also cite its predicate K042221.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · LLZ
58in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LLZ
173in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LLZ
11in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LLZ
116in 2025
MAUDE reports naming product code LLZ, 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 | 76 | 36 | 20 | 152 |
| 2008 | 94 | 52 | 32 | 154 |
| 2009 | 70 | 62 | 21 | 145 |
| 2010 | 51 | 98 | 17 | 145 |
| 2011 | 106 | 79 | 30 | 454 |
| 2012 | 82 | 87 | 12 | 266 |
| 2013 | 95 | 84 | 64 | 1,130 |
| 2014 | 78 | 89 | 6 | 15,631 |
| 2015 | 64 | 90 | 16 | 211 |
| 2016 | 82 | 90 | 12 | 290 |
| 2017 | 78 | 107 | 5 | 104 |
| 2018 | 104 | 105 | 7 | 72 |
| 2019 | 74 | 107 | 2 | 88 |
| 2020 | 81 | 115 | 6 | 82 |
| 2021 | 83 | 116 | 3 | 70 |
| 2022 | 65 | 137 | 4 | 28 |
| 2023 | 87 | 157 | 8 | 26 |
| 2024 | 62 | 131 | 6 | 42 |
| 2025 | 58 | 173 | 11 | 116 |
| 2026 | 45 | 110 | 14 | — |
What is it indicated for?
The Nio 5MP-21" is intended to be used in displaying and viewing digital images, including digital mammography, for review and analysis by trained medical practitioners. The Nio 5MP-21", containing the display MDNG-5121 CB, the software NioWatch and the graphic board BarcoMed Nio, will be marketed as separate device.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062621 · printed Nov 6, 2026
Cite this page
510(k) Report. “K062621: Nio 5MP-21 and MDNG-5121 CB.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062621
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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