510(k) · Cleared
ClearedGUA60A, GU60A-65
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Samsung Electronics Co., Ltd. · KPR System, X-Ray, Stationary
Cleared on Jul 17, 2015 as substantially equivalent to K140332 (Samsung Electronics Co., Ltd., 2014) after a 25-day review. Its family tree reaches back 2 generations to 2013. 20 later devices descend from it.
- Decided
- Jul 17, 2015
- Review
- 25 days
- Class
- Class II
- Product code
- KPR
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K123106 (2013). 20 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK123106 Digital Diagnostic X-Ray System Model Xgeo GU60ASamsung Electronics Co., Ltd. · 2013
- 1 generation backK140332 Xgeo GU60ASamsung Electronics Co., Ltd. · 2014
- This deviceK151685 GUA60A, GU60A-65Samsung Electronics Co., Ltd. · 2015
- Descendant · cites it directly · 19 of its ownK173828 GU60A & GU60A-65Samsung Electronics Co., Ltd. · 2018
- Descendant · 2 generations on · 18 of its ownK180543 GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85Samsung Electronics Co., Ltd. · 2018
- Descendant · 3 generations on · 10 of its ownK181626 Digital Diagnostic Mobile X-ray SystemSamsung Electronics Co., Ltd. · 2018
- Descendant · 3 generations on · 5 of its ownK181631 GR40CWSamsung Electronics Co., Ltd. · 2018
- Descendant · 4 generations on · 4 of its ownK183292 Topaz Mobile DR SystemDRGEM Corporation · 2019
Showing 5 of 20 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 20 · See all- K173828GU60A & GU60A-65Samsung Electronics Co., Ltd. · 2018 · cites it directly19descendants
- K180543GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85Samsung Electronics Co., Ltd. · 2018 · 2 generations on18descendants
- K181626Digital Diagnostic Mobile X-ray SystemSamsung Electronics Co., Ltd. · 2018 · 3 generations on10descendants
- K181631GR40CWSamsung Electronics Co., Ltd. · 2018 · 3 generations on5descendants
- K183292Topaz Mobile DR SystemDRGEM Corporation · 2019 · 4 generations on4descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K123106 | Digital Diagnostic X-Ray System Model Xgeo GU60A | Samsung Electronics Co., Ltd. | 2013 | — |
| −1 | K140332 | Xgeo GU60A | Samsung Electronics Co., Ltd. | 2014 | — |
| 0 (this device) | K151685 | GUA60A, GU60A-65 | Samsung Electronics Co., Ltd. | 2015 | — |
| +1 | K173828 | GU60A & GU60A-65 | Samsung Electronics Co., Ltd. | 2018 | — |
| +2 | K180543 | GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85 | Samsung Electronics Co., Ltd. | 2018 | — |
| +3 | K181626 | Digital Diagnostic Mobile X-ray System | Samsung Electronics Co., Ltd. | 2018 | — |
| +3 | K181631 | GR40CW | Samsung Electronics Co., Ltd. | 2018 | — |
| +4 | K183292 | Topaz Mobile DR System | DRGEM Corporation | 2019 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 7 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2021 | 2 | 0 |
| 2022 | 2 | 0 |
| 2023 | 1 | 0 |
| 2024 | 4 | 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 KPR? 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 KPR device
- #1 K242119 Innovision-Exiiscore 17.0 · 9 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 |
|---|---|---|---|
| * | K140332 | Xgeo GU60ASummary page 4…nostic X-ray System D. Classification Name: Stationary X-ray System E. Regulation: 21 CFR 892.1680 F. Product Code: KPR G. 510(k) Number: K140332 H. 510(k) Decision Date: May 28,2014 7. Device Description The GU60A & GU60A-65 digital X-ray imaging systems… | 2014 |
| † | K150165 | GC85A | 2015 |
What descends from it? (20)
See all 201 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K173828 | GU60A & GU60A-65 | 2018 | 19 |
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 2 years and passes through 1 company; a new generation was cleared every 1.1 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K173828 (Samsung Electronics Co., Ltd., 2018) has gone furthest, with 19 descendants of its own.
How does its category compare?
All KPR devicesKPR System, X-Ray, Stationary: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · KPR
8in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KPR
155in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KPR
7in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KPR
39in 2025
MAUDE reports naming product code KPR, 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 | 12 | 31 | 10 | 120 |
| 2008 | 15 | 48 | 10 | 95 |
| 2009 | 9 | 35 | 5 | 61 |
| 2010 | 9 | 126 | 3 | 82 |
| 2011 | 9 | 152 | 5 | 103 |
| 2012 | 11 | 58 | 1 | 74 |
| 2013 | 5 | 163 | 5 | 24 |
| 2014 | 10 | 108 | 8 | 34 |
| 2015 | 18 | 81 | 1 | 59 |
| 2016 | 11 | 84 | 4 | 18 |
| 2017 | 6 | 75 | 3 | 31 |
| 2018 | 15 | 30 | 4 | 36 |
| 2019 | 12 | 33 | 1 | 77 |
| 2020 | 16 | 39 | 1 | 41 |
| 2021 | 6 | 55 | 0 | 37 |
| 2022 | 8 | 43 | 2 | 27 |
| 2023 | 9 | 76 | 4 | 39 |
| 2024 | 11 | 162 | 1 | 34 |
| 2025 | 8 | 155 | 7 | 39 |
| 2026 | 6 | 197 | 0 | — |
What is it indicated for?
The GU60A & GU60A-65 Digital X-ray Imaging Systems are intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K151685 · printed Nov 4, 2026
Cite this page
510(k) Report. “K151685: GUA60A, GU60A-65.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K151685
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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