510(k) · Cleared
ClearedDX-D Imaging Package
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Agfa Healthcare N.V. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Cleared on Aug 16, 2012 as substantially equivalent to K092669 (Agfa Healthcare N.V., 2009) after a 127-day review. Its family tree reaches back 6 generations to 1981. 3 later devices descend from it.
- Decided
- Aug 16, 2012
- Review
- 127 days
- Class
- Class II
- Product code
- MQB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K803130 (1981). 22 ancestors in all. 3 later devices descend from it, 1 citing it directly.
- Root · 6 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
- 5 generations backK971452 Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc. · 1997 · Recalled
- 4 generations backK983732 Thorax FD and Multix FDSiemens Medical Solutions USA, Inc. · 1999 · Recalled
- 3 generations backK992794 Stingray DR, Model 1Infimed, Inc. · 1999
- 2 generations backK024147 Paxscan 4030 Medical Digital Imaging SystemVarian Medical Systems, Inc. · 2003
- 1 generation backK092669 DX-D Imaging PackageAgfa Healthcare N.V. · 2009 · Recalled
- This deviceK121095 DX-D Imaging PackageAgfa Healthcare N.V. · 2012
- Descendant · cites it directly · 2 of its ownK142184 DX-D Imaging PackageAgfa Healthcare N.V. · 2014
- Descendant · 2 generations on · 1 of its ownK161368 DX-D Imaging Package (DR 10s), DX-D Imaging Package (DR 14s), DX-D…Agfa Healthcare N.V. · 2016
- Descendant · 3 generations on · 0 of its ownK172784 DX-D Imaging PackageAgfa Healthcare N.V. · 2017
Most influential descendants
Showing 3 of 3 · See all- K142184DX-D Imaging PackageAgfa Healthcare N.V. · 2014 · cites it directly2descendants
- K161368DX-D Imaging Package (DR 10s), DX-D Imaging Package (DR 14s), DX-D Imaging Package (DR…Agfa Healthcare N.V. · 2016 · 2 generations on1descendant
- K172784DX-D Imaging PackageAgfa Healthcare N.V. · 2017 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K803130 | Multix U. Bucky Table X-Ray Unit | Siemens Corp. | 1981 | 1 |
| −5 | K971452 | Multix Top/Pro Radiographic X-Ray Table | Siemens Medical Solutions USA, Inc. | 1997 | 8 |
| −4 | K983732 | Thorax FD and Multix FD | Siemens Medical Solutions USA, Inc. | 1999 | 1 |
| −3 | K992794 | Stingray DR, Model 1 | Infimed, Inc. | 1999 | — |
| −2 | K024147 | Paxscan 4030 Medical Digital Imaging System | Varian Medical Systems, Inc. | 2003 | — |
| −1 | K092669 | DX-D Imaging Package | Agfa Healthcare N.V. | 2009 | 1 |
| 0 (this device) | K121095 | DX-D Imaging Package | Agfa Healthcare N.V. | 2012 | — |
| +1 | K142184 | DX-D Imaging Package | Agfa Healthcare N.V. | 2014 | — |
| +2 | K161368 | DX-D Imaging Package (DR 10s), DX-D Imaging Package (DR 14s), DX-D Imaging… | Agfa Healthcare N.V. | 2016 | — |
| +3 | K172784 | DX-D Imaging Package | Agfa Healthcare N.V. | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1986 | 1 | 0 |
| 1988 | 1 | 0 |
| 1992 | 1 | 0 |
| 1994 | 2 | 0 |
| 1995 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 3 | 0 |
| 2000 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 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 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 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 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 |
|---|---|---|---|
| * | K092669 | DX-D Imaging PackageSummary page 2…aphy. D. SUBSTANTIAL EQUIVALENCE SUMMARY Agfa's DX-D Imaging Package has an Indications For Use statement similar to the statements for the predicate device, K092669. Intended uses are the same. The devices have the same technological characteristics. Descriptive characteristics and performance… | 2009 |
| † | K051901 | NIO 3MP-21 | 2005 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K142184 | DX-D Imaging Package | 2014 | 2 |
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 31 years and passes through 5 companies; a new generation was cleared every 3.3 years on median.
- 13 of the 22 ancestors have a recall of any class.
- Of its descendants, K142184 (Agfa Healthcare N.V., 2014) has gone furthest, with 2 descendants of its own.
- 3 other devices also cite its predicate K092669.
How does its category compare?
All MQB devicesMQB Solid State X-Ray Imager (Flat Panel/Digital Imager): FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · MQB
8in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MQB
127in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQB
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQB
141in 2025
MAUDE reports naming product code MQB, 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 | 13 | 22 | 15 | 25 |
| 2008 | 8 | 15 | 36 | 30 |
| 2009 | 15 | 57 | 19 | 34 |
| 2010 | 11 | 116 | 14 | 39 |
| 2011 | 24 | 102 | 10 | 101 |
| 2012 | 22 | 80 | 8 | 267 |
| 2013 | 21 | 105 | 6 | 159 |
| 2014 | 32 | 102 | 0 | 29 |
| 2015 | 21 | 81 | 0 | 21 |
| 2016 | 22 | 92 | 0 | 26 |
| 2017 | 31 | 30 | 1 | 20 |
| 2018 | 16 | 30 | 4 | 84 |
| 2019 | 22 | 30 | 1 | 45 |
| 2020 | 19 | 28 | 4 | 9 |
| 2021 | 21 | 48 | 1 | 26 |
| 2022 | 31 | 48 | 0 | 13 |
| 2023 | 10 | 30 | 0 | 51 |
| 2024 | 8 | 187 | 0 | 91 |
| 2025 | 8 | 127 | 1 | 141 |
| 2026 | 3 | 245 | 1 | — |
What is it indicated for?
Agfa's DX-D Imaging Package is indicated for use in general projection radiographic applications to capture for display diagnostic quality radiographic images of human anatomy. The DX-D Imaging Package may be used wherever conventional screen-film systems may be used.
Agfa's OX-D Imaging Package is not indicated for use in mammography.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K121095 · printed Nov 6, 2026
Cite this page
510(k) Report. “K121095: DX-D Imaging Package.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K121095
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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