510(k) · Cleared
ClearedXplorer 1600
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Imaging Dynamics Company Limited · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Cleared on Sep 17, 2004 after a 50-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 7 later devices descend from it.
- Decided
- Sep 17, 2004
- Review
- 50 days
- Class
- Class II
- Product code
- MQB
- Recalls
- None
- Predicates
- 0
7 later devices descend from it, 3 citing it directly.
- This deviceK042041 Xplorer 1600Imaging Dynamics Company Limited · 2004
- Descendant · cites it directly · 4 of its ownK063039 Xplorer 2200 Digital Radiographic SystemImaging Dynamics Company, Ltd. · 2006
- Descendant · 2 generations on · 2 of its ownK073632 Intuition, Model 0170Arcoma AB · 2008
- Descendant · 3 generations on · 0 of its ownK140683 0180 Intuition, 0072 PrecisionArcoma AB · 2014 · Recalled
- Descendant · 3 generations on · 0 of its ownK121109 Aerodr X70Konica Minolta Medical & Graphic, Inc. · 2012
- Descendant · 2 generations on · 0 of its ownK071401 X3C 2200 Digital Radiographic SystemImaging Dynamics Company, Ltd. · 2007
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K063039Xplorer 2200 Digital Radiographic SystemImaging Dynamics Company, Ltd. · 2006 · cites it directly4descendants
- K073632Intuition, Model 0170Arcoma AB · 2008 · 2 generations on2descendants
- K1406830180 Intuition, 0072 PrecisionArcoma AB · 2014 · 3 generations on0descendants
- K121109Aerodr X70Konica Minolta Medical & Graphic, Inc. · 2012 · 3 generations on0descendants
- K071401X3C 2200 Digital Radiographic SystemImaging Dynamics Company, Ltd. · 2007 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K042041 | Xplorer 1600 | Imaging Dynamics Company Limited | 2004 | — |
| +1 | K063039 | Xplorer 2200 Digital Radiographic System | Imaging Dynamics Company, Ltd. | 2006 | — |
| +2 | K073632 | Intuition, Model 0170 | Arcoma AB | 2008 | — |
| +3 | K140683 | 0180 Intuition, 0072 Precision | Arcoma AB | 2014 | 2 |
| +3 | K121109 | Aerodr X70 | Konica Minolta Medical & Graphic, Inc. | 2012 | — |
| +2 | K071401 | X3C 2200 Digital Radiographic System | Imaging Dynamics Company, Ltd. | 2007 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2007 | 3 | 0 |
| 2008 | 1 | 0 |
| 2012 | 1 | 0 |
| 2014 | 1 | 0 |
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 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?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (7)
3 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)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K063039 (Imaging Dynamics Company, Ltd., 2006) has gone furthest, with 4 descendants of its own.
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.
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?
The Xplorer 1600 is intended for use by a qualified/irained doctor or technologist on 1 both adult and pediatric patients for taking diagnoslic radiographic exposures of the skull, spinal column, chest, sbdomen, extremilies, and other body parts but not mammography. Appflcaflons can be performed with patient sitting, standing or lying inthe prone or supine posilions.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K042041 · printed Nov 5, 2026
Cite this page
510(k) Report. “K042041: Xplorer 1600.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K042041
Report an extraction error
Are you the manufacturer?
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