510(k) Report

510(k) · Cleared

Cleared

Axis-V Monochrome 5 MP Display

K063066510(k) TraditionalCleared Aug 3, 2007301-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

National Display Systems · LLZ System, Image Processing, Radiological

Cleared on Aug 3, 2007 as substantially equivalent to K042221 (Barco NV Barcoview, 2004) and 1 other predicate after a 301-day review. Its family tree reaches back 6 generations to 2000.

Decided
Aug 3, 2007
Review
301 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K001753 (2000). 25 ancestors in all, the oldest K885042 (1988). No later device cites it as a predicate yet.

  1. Root · 6 generations backK001753 Medis 5MP2 Dual-Head Medical Diagnostic Display SystemBarco NV Display Systems · 2000
  2. 5 generations backK013922 Coronis 3MP Medicl Flat Panel Display SystemBarco N.V. · 2002
  3. 4 generations backK023341 Cornis 5MP Medical Flat Panel Display SystemBarco N.V. · 2002
  4. 3 generations backK032202 Dome CX Digital Flat-Panel Display System, Models C2 and C5IPlanar Systems, Inc. · 2003
  5. 2 generations backK040443 Dome CX Digital Flat-Panel Display System, Model C5IDome Imaging Systems, Inc. · 2004
  6. 1 generation backK042221 Coronis 5MP Medical Flat Panel Display SystemBarco NV Barcoview · 2004
  7. This deviceK063066 Axis-V Monochrome 5 MP DisplayNational Display Systems · 2007
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K001753Medis 5MP2 Dual-Head Medical Diagnostic Display SystemBarco NV Display Systems2000—
−5K013922Coronis 3MP Medicl Flat Panel Display SystemBarco N.V.2002—
−4K023341Cornis 5MP Medical Flat Panel Display SystemBarco N.V.2002—
−3K032202Dome CX Digital Flat-Panel Display System, Models C2 and C5IPlanar Systems, Inc.2003—
−2K040443Dome CX Digital Flat-Panel Display System, Model C5IDome Imaging Systems, Inc.2004—
−1K042221Coronis 5MP Medical Flat Panel Display SystemBarco NV Barcoview2004—
0 (this device)K063066Axis-V Monochrome 5 MP DisplayNational Display Systems2007—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199020
199120
199410
199520
199650
199710
199820
200210
200410
200510
FIG. 1 — Lineage of K063066, 2000–2007Source: 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 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? (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
*K042221Coronis 5MP Medical Flat Panel Display System
Summary page 1
…AXIS-V 5MP Monochrome Display H. Classification Number: 21 CFR 892.2050/Procode 9OLLZ 1. Substantial Equivalence: Coronis 5MP (Barco) K042221 RadiForce G51 (Eizo Nanao) K042755 J. Device Description: The AXIS-V 5MP Monoch…
Barco NV Barcoview2004—
*K042755Monochrome LCD Monitor, Radiforce G51
Summary page 1
…: 21 CFR 892.2050/Procode 9OLLZ 1. Substantial Equivalence: Coronis 5MP (Barco) K042221 RadiForce G51 (Eizo Nanao) K042755 J. Device Description: The AXIS-V 5MP Monochrome Display is a diagnostic displa…
Eizo Nanao Corporation2005—

Also cleared against K042221: 3 other devices →

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 7 years and passes through 6 companies; a new generation was cleared every 11 months on median.
  • None of the 25 ancestors has a recall.
  • 3 other devices also cite its predicate K042221.

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. 2007, 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 AXIS-V 5MP Radiological Monochrome Medical Display is intended to be used to display and view digital images, including digital mammography, for review and analysis by trained medical practitioners.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063066: Axis-V Monochrome 5 MP Display.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K063066

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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