510(k) · Cleared
Recalled · 2012DX-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 Nov 6, 2009 as substantially equivalent to K090672 (Agfa Healthcare N.V., 2009) and 1 other predicate after a 67-day review. Its family tree reaches back 5 generations to 1981. 34 later devices descend from it. It has been recalled once.
- Decided
- Nov 6, 2009
- Review
- 67 days
- Class
- Class II
- Product code
- MQB
- Recalls
- 1
- Predicates
- 2
Its longest line of descent runs back 5 generations to K803130 (1981). 21 ancestors in all. 34 later devices descend from it, 4 citing it directly.
- Root · 5 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
- 4 generations backK971452 Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc. · 1997 · Recalled
- 3 generations backK983732 Thorax FD and Multix FDSiemens Medical Solutions USA, Inc. · 1999 · Recalled
- 2 generations backK992794 Stingray DR, Model 1Infimed, Inc. · 1999
- 1 generation backK024147 Paxscan 4030 Medical Digital Imaging SystemVarian Medical Systems, Inc. · 2003
- This deviceK092669 DX-D Imaging PackageAgfa Healthcare N.V. · 2009
- Descendant · cites it directly · 25 of its ownK122736 DX-D Imaging PackageAgfa Healthcare N.V. · 2013
- Descendant · 2 generations on · 15 of its ownK140771 Philips Eleva WorkspotPhilips Medical Systems Dmc GmbH · 2014
- Descendant · cites it directly · 8 of its ownK103050 DX-D 300Agfa Healthcare N.V. · 2010
- Descendant · 2 generations on · 7 of its ownK141192 DR 400Agfa Healthcare N.V. · 2014
- Descendant · 2 generations on · 7 of its ownK112670 DX-D 600Agfa Healthcare N.V. · 2011 · Recalled
Showing 5 of 34 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 34 · See all- K122736DX-D Imaging PackageAgfa Healthcare N.V. · 2013 · cites it directly25descendants
- K140771Philips Eleva WorkspotPhilips Medical Systems Dmc GmbH · 2014 · 2 generations on15descendants
- K103050DX-D 300Agfa Healthcare N.V. · 2010 · cites it directly8descendants
- K141192DR 400Agfa Healthcare N.V. · 2014 · 2 generations on7descendants
- K112670DX-D 600Agfa Healthcare N.V. · 2011 · 2 generations on7descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K803130 | Multix U. Bucky Table X-Ray Unit | Siemens Corp. | 1981 | 1 |
| −4 | K971452 | Multix Top/Pro Radiographic X-Ray Table | Siemens Medical Solutions USA, Inc. | 1997 | 8 |
| −3 | K983732 | Thorax FD and Multix FD | Siemens Medical Solutions USA, Inc. | 1999 | 1 |
| −2 | K992794 | Stingray DR, Model 1 | Infimed, Inc. | 1999 | — |
| −1 | K024147 | Paxscan 4030 Medical Digital Imaging System | Varian Medical Systems, Inc. | 2003 | — |
| 0 (this device) | K092669 | DX-D Imaging Package | Agfa Healthcare N.V. | 2009 | — |
| +1 | K122736 | DX-D Imaging Package | Agfa Healthcare N.V. | 2013 | — |
| +2 | K140771 | Philips Eleva Workspot | Philips Medical Systems Dmc GmbH | 2014 | — |
| +1 | K103050 | DX-D 300 | Agfa Healthcare N.V. | 2010 | — |
| +2 | K141192 | DR 400 | Agfa Healthcare N.V. | 2014 | — |
| +2 | K112670 | DX-D 600 | Agfa Healthcare N.V. | 2011 | 4 |
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 |
|---|---|---|
| 2010 | 1 | 0 |
| 2011 | 2 | 0 |
| 2012 | 1 | 0 |
| 2013 | 1 | 0 |
| 2014 | 5 | 0 |
| 2015 | 2 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2019 | 3 | 0 |
| 2020 | 2 | 0 |
| 2021 | 7 | 0 |
| 2023 | 2 | 0 |
| 2024 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K090672 | Agfa Computed Radiography Systems with NX WorkstationsSummary page 1…his is a 510(k) for Agfa’s DX-D Imaging Package. The predicate devices are two devices with similar technology: Agfa’s Computed Radiography Systems with NX Workstations (K090672) and Varian Medical’s PaxScan 4030 (K024147). B. DEVICE DESCRIPTION The new device is a direct radiography imaging system of si… | 2009 |
| * | K024147 | Paxscan 4030 Medical Digital Imaging SystemSummary page 1…age. The predicate devices are two devices with similar technology: Agfa’s Computed Radiography Systems with NX Workstations (K090672) and Varian Medical’s PaxScan 4030 (K024147). B. DEVICE DESCRIPTION The new device is a direct radiography imaging system of similar design and construction to the predxca… | 2003 |
What descends from it? (34)
See all 344 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 16, 2012 | Not classified | Z-1062-2012 | Device Design | The firm received a complaint that when using the DX-D Mobile DR X-Ray unit they noticed the detector cable was hot. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 28 years and passes through 5 companies; a new generation was cleared every 3.3 years on median.
- 12 of the 21 ancestors have a recall of any class.
- Of its descendants, K122736 (Agfa Healthcare N.V., 2013) has gone furthest, with 25 descendants of its own.
- 2 other devices also cite its predicate K090672.
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. 2009, 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 providing diagnostic quality images to aid the physician with diagnosis.
Systems can be used with MUSICA® image processing to create radiographic images of the skeleton (including skull, spinal column and extremities) chest, abdomen and other body parts.
Agfa’s DX-D Imaging Package is not indicated for use in mammography.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K092669 · printed Nov 4, 2026
Cite this page
510(k) Report. “K092669: DX-D Imaging Package.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K092669
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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